WO2011126917A1

WO2011126917A1 - Monophosphorus ligands and their use in cross-coupling reactions

Info

Publication number: WO2011126917A1
Application number: PCT/US2011/030681
Authority: WO
Inventors: Nizar Haddad; Bo QU; Sonia Rodriguez; Chris Senanayake; Wenjun Tang; Xudong Wei; Nathan K. Yee
Original assignee: Boehringer Ingelheim International GmbH
Current assignee: Boehringer Ingelheim International GmbH
Priority date: 2010-04-05
Filing date: 2011-03-31
Publication date: 2011-10-13
Anticipated expiration: 2012-10-05
Also published as: EP2556077A1; US20130137902A1; JP5803042B2; EP2556077B1; JP2013523813A; US9096626B2

Abstract

Phosphine ligands of the formula Ia, IB and mixtures thereof.

Description

Monophosphorus Li2ands And Their Use In Cross- Couplin2 Reactions

BACKGROUND OF THE INVENTION

1. TECHNICAL FIELD

The present invention relates to a series of novel P-chiral monophosphorus ligands derived from a dihydrobenzo[l,3]oxaphosphole framework and their metal complexes as catalysts for applications in cross-coupling reaction. More particularly, the present invention relates to these phosphine ligands and their related catalysts for transition metal catalyzed cross- coupling reactions including carbon-carbon bond forming reactions and C-X cross- coupling reactions.

2. BACKGROUND INFORMATION

Metal-catalyzed cross-coupling has become one of the most important transformations in organic chemistry. A. de Meijere, F. Diederich, Eds. Metal-Catalyzed Cross-Coupling Reactions, Vol. 2: Wiley-VCH, Weinheim, 2004. J.-P. Corbet, G. Mignani, Chem. Rev. 2006, 106, 2651. Development of efficient chiral or nonchiral ligands for metal-catalyzed cross-coupling has gained particular attention in the latest twenty years. As ligands have played essential roles during each step of the catalytic cycle including oxidative addition, transmetallation, and reductive elimination, the steric and electronic properties of ligand can greatly influence the rate, regioselectivity, and stereoselectivity of the cross-coupling reaction. Recent advances pioneered by Buchwald (T. E. Barder, S. D. Walker, J. R. Martinelli, S. L. Buchwald, /. Am. Chem. Soc. 2005, 127, 4685; S. D. Walker, T. E. Barder, J. R. Martinelli, S. L. Buchwald, Angew. Chem., Int. Ed. 2004, 43, 1871 ; K. Billingsley, S. L. Buchwald, /. Am. Chem. Soc. 2007, 129, 3358; S. L. Buchwald, B. P. Fors, D. S. Surry, WO2009/076622), Hartwig (J. F. Hartwig, Q. Shelby, N. Kataoka, WO 2002/011883; M. Driver, J. F. Hartwig, /. Am. Chem. Soc. 1996, 118, 7217), Fu (M. R. Netherton, C. Dai, K. Neuschuta, G. C. Fu, /. Am. Chem. Soc. 2001, 123, 10099; J. H. Kirchoff, M. R. Netherton, I. D. Hills, G. C. Fu, /. Am. Chem. Soc. 2002, 124, 13662), and Beller et al (A. Zapf, A, Ahrentraut, M. Beller Angew. Chem., Int. Ed. 2000, 39, 4153; A. Ahrentraut, A. Zapf, M. Beller, Adv. Synth. Catal. 2002, 344, 209; A. Zapf, R. Jackstell, F. Rataboul, T. Riermeier, A. Monsees, C. Fuhrmann, N. Shaikh, U. Dingerdissen, M. Beller, Chem. Comm. 2004, 38) have led to the development of many efficient ligands for cross-coupling reactions including carbon-carbon bond forming

:

The Suzuki-Miyaura coupling has become one of most useful method for formation of carbon-carbon bonds and has been used in numerous synthetic ventures. (N. Miyaura, Topics in Current Chem. 2002, 219, 11 ; A. Suzuki, Organomet. Chem. 1999, 576, 147). Despite the recent advances on this reaction, the Suzuki-Miyaura coupling of sterically hindered substrates and further decrease of the catalyst loading remain great challenges. Development of new ligands for Suzuki-Miyaura coupling reaction remains imperative to further increase its efficiency and expand its substrate scope.

BRIEF SUMMARY OF THE INVENTION

The invention provides a series of novel and efficient chiral monophosphorus ligands derived from a dihydrobenzo[l ,3]oxaphosphole framework that has shown superior results for Suzuki coupling or asymmetric Suzuki reaction. High reactivity and selectivity have been observed in a sterically-congested asymmetric Suzuki coupling.

DETAILED DESCRIPTION OF THE INVENTION

In its first aspect, the present invention provides compounds of the formula (la), (lb), or a mixture thereof:

wherein:

R is (Ci-C6)-alkyl, CF₃, (C3-Cio)-carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl, or ferrocenyl, wherein each such (C3-

Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 11- membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl, and CF₃;

R¹, R², R³, R⁴, R⁵ are each independently selected from the group consisting of H, halo, CF₃, -0(Ci-C₆)alkyl, (Ci-C₆)alkyl, (C₃-Ci₀)carbocyclyl, (5- to 11- membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl, -NRⁿR¹², - Si(Rⁿ)3 and -SR¹¹, wherein each such (C3-Cio)carbocyclyl, (5- to I lmembered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 1 l-membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl and CF₃; or any two adjacent instances of R¹, R², R³, R⁴, R⁵, taken together with the carbons to which they are bound, form a five- or six-membered substituted or unsubstituted aryl or heteroaryl ring; provided that at least one of R¹, R², R³, R⁴, R⁵ are OR¹¹ ;

R⁶, R⁷, R⁸ are each independently selected from the group consisting of H, CF₃, -0(Ci- C₆)alkyl, (Ci-C6)alkyl, (C3-Cio)carbocyclyl, (5- to 11 -membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl and -NRⁿR¹²; wherein each such (C3- Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 11- membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl, and CF₃; R⁹, R¹⁰ are each independently selected from the group consisting of H, (Ci-C6)alkyl,

(C3-C6)cycloalkyl, (3- to 6-membered)heterocycloalkyl, (C6-Cio)aryl, (5- to 6- membered)heteroaryl, and -SiR⁵3 ; wherein each such (C3-C6)cycloalkyl, (3- to 6- membered)heterocycloalkyl, (C6-Cio)aryl or (5- to 6-membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C₆)alkyl, (Ci-C₆)alkyl, and CF₃;

R¹¹ and R¹² are each independently selected from the group consisting of H, (Ci- C₆)alkyl, CF₃, (C3-Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C₆- Cio)aryl, and (5 to l l-membered)heteroaryl, wherein each such (C3-Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 11 -membered)heteroaryl group is optionally independently substituted with 1 to 3 substituents independently selected from the group consisting of halo, -0(Ci-C6)alkyl, (Ci-C6)alkyl, and -CF₃.

In a second aspect, the invention relates to compounds of formula (la), (lb), or a mixture thereof, wherein R is -(Ci-C6)alkyl selected from -CH₃, -CH₂CH₃, -CH(CH₃)₂,

-C(CH₃)₃, -C(CH₂CH₃)3, and -C(CH₂CH3)(CH₃)₂, and R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, Rⁿ and R¹² are as defined in the first aspect.

In a third aspect, the invention provides compounds of the formula (la), (lb), or a mixture thereof, wherein R is -(C3-Cio)carbocyclyl selected from cyclopentyl, cyclohexyl, and 1-adamantyl, and R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R¹² are as defined in the first aspect.

In a fourth aspect, the invention provides compounds of the formula (la), (lb), or a mixture thereof, wherein R is -(C₆-Cio)aryl selected from phenyl, ortho-tolyl, para- tolyl, 3,5-dimethylphenyl, 3,5-di-i-butylphenyl, 3,5-di-CF₃-phenyl, ortho-CF₃-phenyl, ortho-anisyl, and naphthyl, and R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R¹² are as defined in the first aspect.

In a fifth aspect, the invention provides compounds of the formula (la), (lb), or a mixture thereof, wherein R¹, R², R³, R⁴, R⁵ are each independently H, -CH₃, -CH₂CH₃,

-CH(CH₃)₂, -C(CH₃)₃, -OCH3, -OCH₂CH₃, -OCH(CH₃)₂, N(CH₃)₂, N(CH₂CH₃)₂, or SiMe_3, , and R, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R¹² are as defined in the first, second, third or fourth aspect. In a sixth aspect, the invention provides compounds of the formula (la), (lb), or a mixture thereof, wherein R⁶, R⁷, R⁸ are H, and R, R¹, R², R³, R⁴, R⁵, R⁹, R¹⁰, R¹¹ and R¹² are as defined in the first, second, third, fourth or fifth aspect.

In a seventh aspect, the invention provides compounds of the formula (la), (lb), or a mixture thereof, R⁹ and R¹⁰ are each independently H, -CH , -CH₂CH , -CH(CH )₂,

-C(CH₃)₃, phenyl, ortho-tolyl, para-tolyl, 3,5-dimethylphenyl, 3,5-di-i-butylphenyl, 3,5-di-CF₃-phenyl, ortho-CF₃-phenyl, ortho-anisyl, 2,6-dimethoxyphenyl or naphthyl, and R, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R¹¹ and R¹² are as defined in the first, second, third, fourth, fifth aspect or sixth aspect.

In an eighth aspect, the invention provides a phosphine ligand having the formula (Ila) or (lib), or a mixture thereof,

(Ila) (lib)

wherein:

R is -CH(CH₃)₂, -C(CH₃)₃ -C(CH₂CH₃)(CH₃)_2, cyclohexyl, 1 -adamantyl, phenyl, ortho- tolyl, 3,5-xylyl, ortho-anisyl, or ferrocenyl; and R¹, R², and R³ are independently H, -CH₃, -CH₂CH₃, -CH(CH₃)₂, -C(CH₃)₃, -OCH₃, -OCH₂CH_3, -OCH(CH₃)₂, OPh, N(CH₃)₂, N(CH₂CH₃)₂, SiMe₃, CF₃.

More particularly, the invention provides phosphine ligands selected from the group consisting of:

(S) and (/?)-3-tert-butyl-4-phenyl-2,3-dihydrobenzo[if|[l ,3]oxaphosphole,

(5") and («)-3-tert-butyl-4-(2,6-dimethoxyphenyl)-2,3- dihydrobenzo[<i][l ,3]oxaphosphole,

(5") and («)-2-(3-tert-butyl-2,3-dihydrobenzo[i/][l ,3]oxaphosphol-4-yl)-Nl ,Nl ,N3,N3- tetramethylbenzene- 1 ,3-diamine,

(5") and (7?)-2-(3-tert-butyl-2,3-dihydrobenzo[d] [l ,3]oxaphosphol-4-yl)-N,N- dimethylaniline,

(S) and (/?)-3-tert-butyl-4-(2-methoxyphenyl)-2,3-dihydrobenzo[d] [l ,3]oxaphosphole,

(S) and (/?)-3-tert-butyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole,

(5") and («)-3-tert-butyl-4-(2,4,6-triisopropylphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole,

(S) and (/?)-3-tert-butyl-4-o-tolyl-2,3-dihydrobenzo[d][l ,3]oxaphosphole,

(S) and (/?)-3-tert-butyl-4-(2-phenoxyphenyl)-2,3-dihydrobenzo[d] [l ,3]oxaphosphole,

(S) and (/?)-3-cyclohexyl-4-phenyl-2,3-dihydrobenzo[d][l ,3]oxaphosphole, (S) and (R)-

3 -cyclohexyl-4- (2 , 6-dimethoxyphenyl) -2 , 3 -dihydrobenzo [d] [ 1 , 3 ] oxaphosphole, (S) and

(«)-2-(3-cyclohexyl-2,3-dihydrobenzo[d] [l ,3]oxaphosphol-4-yl)-Nl ,Nl ,N3,N3- tetramethylbenzene- l ,3-diamine, , (S) and ( ?)-2-(3-cyclohexyl-2,3- dihydrobenzo[d] [l ,3]oxaphosphol-4-yl)-N,N-dimethylaniline,

(S) and (/?)-3-cyclohexyl-4-(2-methoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole,

(S) and (/?)-3-cyclohexyl-4-(2,4,6-triisopropylphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole,

(S) and (/?)-3-cyclohexyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole, (5) and (R)-3- cyclohexyl-4-o-tolyl-2,3-dihydrobenzo[d][l ,3]oxaphosphole, and (S) and (R)-3- cyclohexyl-4-(2-phenoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole. The present invention further provides a catalyst prepared by a process including contacting a transition metal salt, or a complex thereof, and a chiral ligand according to the present invention as described.

The present invention further provides a process for preparation of a chiral or nonchiral compound by employing a ligand or catalyst according to the present invention as described herein above.

In another aspect, the present invention provides a process for preparation of the above- described ligands of formulas la, lb, Ila and lib. In general, these ligands may be prepared in the manner depicted in the general reaction scheme below.

Scheme 1

As illustrated in Scheme 1 , phenol Ilia, or its enantiomer, or a mixture of thereof is converted into a triflate IVa, or its enantiomer, or a mixture of thereof, by reacting with Tf₂NPh or trifluoromethylsulfonyl anhydride in a suitable solvent such as

dichloromethane, THF, or toluene. Cross-coupling of triflate IVa with a boronic acid of formula V with a catalytic amount of a palladium precursor such as Pd(OAc)₂ or Pd₂dba3 and a suitable phosphorus ligand such as S-Phos, Cy₃P, or a ligand of formula la described in this invention, provides the biaryl product of formula Via. Reduction of this phosphine oxide Via under a reaction condition of polymethylhydrosiloxane (PMHS)/Ti(0 Pr)4, PhSiI¾, HSiCl₃/Et N, or DIBAL, provides the ligand of formula la, or its enantiomer, or a mixture of thereof.

Starting compounds of the formula Ilia may be made in the manner described by Tang et al., Organic Letters, Vol. 12, No. 1, pp 176-179 (2010) and Tang et al., Organic Letters, Vol. 12, No. 5, pp 1104-1107 (2010). The process for making the ligands of the invention may be better understood by having reference to the following examples.

Example 1 : (5^,)-3-ieri-butyl-2,3-dihydrobenzo[<i][l,3]oxaphosphol-4-yl trifluoromethanesulfonate oxide

To a solution of (5^,)-3-ieri-butyl-2,3-dihydrobenzo[<i][l,3]oxaphosphol oxide -4-ol (50 mg, 0.221 mmol) and triethylamine (89 mg, 0.88 mmol, 4 equiv) in CH₂C1₂ (2 mL) at 0 °C was added Tf₂NPh (96 mg, 0.27 mmol, 1.2 equiv) over 1 min. The mixture was stirred at rt for 2 h and then quenched with addition of water (2 mL). The CH₂C1₂ layer was separated, dried over sodium sulfate, concentrated, and purified by silica gel column chromatography (eluents: hexanes to EtOAc) to provide (5)-3-ieri-butyl-2,3- dihydrobenzo[<i][l,3]oxaphosphol-4-yl trifluoromethanesulfonate oxide (75 mg, 0.21 mmol, 95%) as white solid. *HNMR (500 MHz, CD₂C1₂) δ 7.58 (t, J = 8.3 Hz, 1H), 7.03 (dd, J = 8.2, 3.5 Hz, 1H), 7.00 (dd, J = 8.5, 2.4 Hz, 1H), 4.67 (dd, J = 14.2, 2.1 Hz, 1H), 4.46 (dd, / = 14.1, 11.1 Hz, 1H), 1.21 (d, / = 16.8 Hz, 9H); ³¹PNMR (202 MHz, CD₂C1₂) δ 75.6; ¹³CNMR (125 MHz, CD₂C1₂) 167.1 (d, J = 16.8 Hz), 150.0, 137.1, 120.3, 117.8, 114.7 (d, / = 4.4 Hz), 114.2 (d, /

24.2; ESI-MS: m/z 359 [M +H]⁺.

Example 2: (5')-3-tert-butyl-4-(2,6-dimethoxyphi dihydrobenzo[if|[l,3]oxaphosphole oxide by Suzuki coupling with S-phos as the ligand

To a solution of (5^,)-3-ieri-butyl-2,3-dihydrobenzo[<i][l,3]oxaphosphol-4-yl trifluoromethanesulfonate oxide (5 g, 13.9 mmol) and 2,6-dimethoxyphenylboronic acid (3.8 g, 20.9 mmol, 1.5 equiv), Pd₂dba₃ (383 mg, 0.42 mmol, 3 mol ), S-Phos (1.15 g,

2.79 mmol, 20 mol ) and KF (3.24 g, 55.8 mmol, 4 equiv) was charged degassed dioxane (30 mL). The mixture was stirred under nitrogen at 100 °C for 12 h. The mixture was cooled to rt and concentrated. To the residue was added DCM (30 mL) and 2 N NaOH (30 mL). The DCM layer was further washed with 2 N NaOH (30 mL) and brine (30 mL), dried over sodium sulfate, and concentrated. The residue was purified by column chromatography (hexane to EtOAc/MeOH 2/1) to provide the desired product as yellow solid (3 g, 8.66 mmol, 62 ^ .'HNMR (500 MHz, CDC1₃): δ= 7.46 (t, / = 7.9 Hz, 1H), 7.28 (t, / = 8.4 Hz, 1H), 6.89 (m, 2H), 6.64 (d, / = 8.4 Hz, 1H), 6.55 (d, / = 8.4 Hz, 1H), 4.47 (dd, / = 13.8, 1.8 Hz, 1H), 4.34 (dd, / = 13.7, 10.5 Hz, 1H), 3.77 (s, 3H), 3.70 (s, 3H), 0.87 (d, 7 = 15.9 Hz, 9H); ³¹PNMR (202 MHz, CDC1₃): δ= 62.4; ¹³CNMR (125 MHz, CDCI₃): S= 165.2 (d, / = 18.8 Hz), 158.5, 157.3, 138.1 (d, / = 6.3 Hz), 134.0 (d, / = 1.3 Hz), 129.8, 125.0 (d, J = 8.8 Hz), 117.4 (d, J = 2.5 Hz), 114.8, 114.0, 112.4 (d, J = 5.0 Hz), 104.3, 103.1, 65.3 (d, J = 60.0 Hz), 55.8, 55.3, 33.4 (d, 7 = 71.3 Hz), 23.6 (d, J = 1.3 Hz); ESI-MS: m/z 347 [M +H]⁺. Example 3: (5')-3-tert-butyl-4-(2,6-dimethoxyphenyl)-2,3- dihydrobenzo[if|[l,3]oxaphosphole oxide by Suzuki coupling with (/?)-3-ieri-butyl-4-(2,6- dimethoxyphenyl)-2,3-dihydrobenzo[if|[l,3]oxaphosphole as the ligand

To a mixture of (5')-3-ieri-butyl-2,3-dihydrobenzo[d][l,3]oxaphosphol-4-yl rifluoromethanesulfonate oxide (215 g, 600 mmol) and 2,6-dimethoxyphenylboronic acid (164 g, 900 mmol, 1.5 equiv), Pd₂dba₃ (6.9 g, 7.5 mmol, 0.0125 equiv), («)-3-ieri-butyl-4- (2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole (5.9 g, 18 mmol, 0.03 equiv) and KF (139 g, 2.4 mol, 4 equiv) was charged degassed dioxane (2 L). The mixture was stirred under nitrogen at 100 °C for 3 h, then cooled to rt and concentrated to remove most dioxane. To the residue was added DCM (1000 mL) and 2 N NaOH (500 mL). The DCM layer was further washed with 2 N NaOH (500 mL) and brine (500 mL), dried over sodium sulfate, and concentrated. The residue was purified by column chromatography (eluent: hexane to EtOAc/MeOH 2/1) to provide the desired product (5)-3-tert-butyl-4- (2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole oxide (190 g, 576 mmol, 91 ) as white solid.

Example 4: (/?)-3-tert-butyl-4-(2,6-dimethoxyphi

dihydrobenzo[d] [ 1 ,3]oxaphosphole

To a solution of (5)-3-tert-butyl-4-(2,6-dimethoxyphenyl)-2,3- dihydrobenzo[d][l,3]oxaphosphole oxide (6.5 g, 18.8 mmol) in THF (65 mL) at rt was added PMHS (13 g) and Ti(0 Pr)4 (6.4 g, 22.5 mmol, 1.2 equiv). The mixture was stirred at reflux for 12 h, then concentrated under vacuum to remove most THF. To the residue treated carefully with 30% NaOH solution (60 mL). Gas was generated during addition. The resulting mixture was further stirred at 60 °C for 0.5 h. To the mixture at rt was added MTBE (60 mL). The MTBE layer was separated and the aqueous layer was washed with MTBE under nitrogen. The MTBE solution was dried, concentrated, and purified by passing through a neutral alumina plug to give the desired product as white crystalline solid (5 g, 15.1 mmol, 81%). *HNMR (400 MHz, CDC1₃): δ = 7.29 (m, 2H), 6.87 (m, 2H), 6.65 (d, / = 8.2 Hz, 1H), 6.59 (d, / = 8.3 Hz, 1H), 4.81 (dd, / = 12.5, 1.8 Hz, 1H), 4.53 (dd, J = 25.2, 12.5 Hz, 1H), 3.77 (s, 3H), 3.71 (s, 3H), 0.73 (d, / = 12.1 Hz, 9H); ³¹PNMR (162 MHz, CDCI₃): δ= -7.9; ¹³CNMR (100 MHz, CDC1₃): δ= 163.4, 157.9. 157.1, 138.4 (d, / = 22.3 Hz), 130.5, 129.0, 125.0 (d, / = 16.4 Hz), 123.8 (d, / = 5.4 Hz), 119.6, 109.5, 104.5, 103.6, 70.4 (d, / = 33.8 Hz), 55.9, 55.4, 30.9 (d, / = 23.2 Hz), 26.6 (d, / = 18.1 Hz); ESI- MS: m/z 331 [M +H]⁺.

Example 5: (5')-3-ieri-butyl-4-phenyl-2,3-dihydrobenzo[if|[l,3]oxaphosphole oxide (5')-3-ieri-butyl-4-phenyl-2,3-dihydrobenzo[(i][l,3]oxaphosphole oxide was prepared under a similar condition described in Example 3: 90% yield; 'HNMR (400 MHz, CDC1₃): δ = 7.76 (d, J = 7.4 Hz, 1H), 7.41-7.53 (m, 3H), 7.36 (m, 1H), 7.05 (dd, J = 7.5, 3.6 Hz, 1H), 6.91 (dd, / = 8.3, 3.2 Hz, 1H), 4.56 (dd, / = 13.7, 1.1 Hz, 1H), 4.44 (dd, / = 13.8, 10.5 Hz, 1H), 0.78 (d, / = 16.1 Hz, 9H); ³¹PNMR (162 MHz, CDC1₃): δ= 65.1; ¹³CNMR (100 MHz, CDC1₃): δ= 165.7 (d, / = 19.2 Hz, 1H), 146.7 (d, / = 5.8 Hz, 1H), 134.8 (d, / = 1.7 Hz, 1H), 129.6, 128.5, 128.3, 123.4 (d, / = 8.0 Hz), 112.5 (d, / = 5.3 Hz), 112.4 (d, / = 87.9 Hz), 65.2 (d, / = 61.7 Hz), 33.8 (d, / = 70.7 Hz), 23.7. ESI-MS: m/z 287 [M +H]⁺.

Example 6: (/?)-3-ieri-butyl-4-phenyl-2,3-dihydrobenzo[if|[l,3]oxaphosphole

(/?)-3-ieri-butyl-4-phenyl-2,3-dihydrobenzo[(i][l,3]oxaphosphole was prepared under a similar condition describled in Example 4. 89%; *HNMR (400 MHz, CD₂C1₂): δ= 7.71

(m, 2H), 7.42 (m, 2H), 7.35 (m, 2H), 6.99 (m, 1H), 6.90 (dd, / = 8.1, 0.8 Hz, 1H), 4.87 (dd, / = 12.7, 1.9 Hz, 1H), 4.57 (dd, 7 = 25.9, 12.7 Hz, 1H), 0.64 (d, / = 12.1 Hz, 9H); ³¹PNMR (162 MHz, CD₂C1₂): δ= -11.2; ¹³CNMR (100 MHz, CD₂C1₂): δ= 164.8, 146.5, 143.1, 131.9, 129.9, 129.8, 128.9, 127.9, 122.7 (d, / = 17.9 Hz), 122.3 (d, 7 = 3.1 Hz), 110.5, 70.5 (d, / = 26.9 Hz), 32.1 (d, / = 20.2 Hz), 27.0 (d, / = 13.8 Hz).

Example 7: (5')-2-(3-tert-butyl-2,3-dihydrobenzo[d][l,3]oxaphosphol-oxide-4-yl)-N,N- dimethylaniline (5')-2-(3-tert-butyl-2,3-dihydrobenzo[d][l,3]oxaphosphol-oxide-4-yl)-N,N-dimethylaniline was prepared under a similar condition described in Example 3: 76% yield; 'HNMR (400 MHz, CDC1₃): δ = 7.74 (br s, 1H), 7.44 (t, 7 = 7.6 Hz, 1H), 7.37 (br s, 1H), 7.29 (dd, 7 = 8.0, 1.8 Hz), 7.03 (m, 1H), 7.01 (d, 7 = 8.1 Hz, 1H), 6.87 (dd, 7 = 9.1, 3.2 Hz, 1H), 4.54 (dd, 7 = 13.9, 2.0 Hz, 1H), 4.41 (dd, 7 = 13.8, 10.7 Hz, 1H), 2.59 (s, 6H), 0.88 (d, 7 = 16.1 Hz, 9H); ³¹PNMR (162 MHz, CDC1₃): δ= 64.1 ; ¹³CNMR (100 MHz, CDC1₃): δ= 145.6 (d, 7 = 5.5 Hz), 134.3, 133.4, 129.3, 124.1 (d, 7 = 8.1 Hz), 121.2, 118.0, 112.1 (d, 7 = 5.2 Hz), 65.5 (d, 7 = 61.7 Hz), 43.4, 33.9 (d, 7 = 71.3 Hz), 24.1 ; ESI-MS: m/z 330 [M +H]⁺.

Example 8: («)-2-(3-tert-butyl-2,3-dihydrobenzo[d][l,3]oxaphosphol-4-yl)-N,N- dimethylaniline

(/?)-2-(3-tert-butyl-2,3-dihydrobenzo[d][l,3]oxaphosphol-4-yl)-N,N-dimethylaniline was prepared under a similar condition describled in Example 4: 63% yield; ^JHNMR (400 MHz, CD₂CI₂): δ= 7.32 (t, 7 = 7.7 Hz, 1H), 7.32 (br s, 1H), 7.24 (m, 1H), 7.04 (br s, 1H), 6.99 (dd, 7 = 8.2, 1.0 Hz, 1H), 6.93 (dt, 7 = 7.4, 1.2 Hz, 1H), 6.83 (dd, 7 = 8.1, 0.9 Hz, 1H), 4.80 (dd, 7 = 12.5, 1.8 Hz, 1H), 4.50 (dd, 7 = 26.2, 12.6 Hz, 1H), 2.55 (s, 6H), 0.63 (d, 7 = 11.9 Hz, 9H); ³¹PNMR (162 MHz, CD₂C1₂): δ= -7.2; ¹³CNMR (100 MHz, CD₂C1₂): δ= 151.4, 133.1, 133.0, 131.8, 131.5, 129.3, 128.9, 122.7, 122.6, 121.1, 118.5, 109.7, 70.9 (d, 7 = 27.9 Hz), 43.4, 31.7 (d, 7 = 20.6 Hz), 27.3 (d, 7 = 14.7 Hz); ESI-MS: m/z 314 [M +H]⁺.

L

Example 9: (5')-3-tert-butyl-4-(2-methoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole oxide ((5')-3-tert-butyl-4-(2-methoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole oxide was prepared under a similar condition described in Example 3: 85%; 'HNMR (500 MHz, CDC1₃): δ = 7.61 (d, J = 7.3 Hz, 1H), 7.44 (t, J = 8.0 Hz, 1H), 7.34 (t, J = 7.6 Hz, 1H),

7.05 (m, 2H), 6.95 (d, J = 8.2 Hz, 1H), 6.90 (dd, J = 8.3, 3.2 Hz, 1H), 4.51 (dd, J = 13.8,

1.6 Hz, 1H), 4.41 (dd, J = 13.8, 10.5 Hz, 1H), 3.79 (s, 3H), 0.82 (d, J = 16.1 Hz, 9H); ³¹PNMR (202 MHz, CDC1₃): δ= 63.6; ¹³CNMR (125 MHz, CDC1₃): δ= 165.5 (d, J = 19.1

Hz), 156.4, 142.3 (d, / = 5.7 Hz), 133.7 (d, J = 1.6 Hz), 132.7, 129.7, 128.8 (d, J = 2.3 Hz), 125.0 (d, / = 8.2 Hz), 120.5, 113.6 (d, J = 89.4 Hz), 112.2 (d, / = 5.4 Hz), 110.7, 65.4 (d, J = 61.1 Hz), 55.4, 33.6 (d, 7 = 71.1 Hz), 23.9 (d, / = 1.1 Hz); ESI-MS: m/z 317 [M +H]⁺.

Example 10: (/?)-3-tert-butyl-4-(2-methoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole

(/?)-3-tert-butyl-4-(2-methoxyphenyl)-2,3-dihydrobenzo[d][l,3]oxaphosphole was prepared under a similar condition describled in Example 4: 78%; 'HNMR (500 MHz, CD2CI2): δ = 7.41 (d, J = 7.4 Hz, 1H), 7.33 (m, 1H), 7.29 (t, J = 7.9 Hz, 1H), 7.00 (m, 2H), 6.94 (dd, J = 7.4, 3.2 Hz, 1H), 6.87 (d, J = 8.4 Hz, 1H), 4.83 (dd, J = 12.6, 1.9 Hz, 1H), 4.54 (dd, J = 25.7, 12.6 Hz, 1H), 3.78 (s, 3H), 0.67 (d, J = 12.1 Hz, 9H); ³¹PNMR (202 MHz, CD2CI2): δ= -9.9; ¹³CNMR (125 MHz, CD₂C1₂): δ= 164.4, 157.1, 143.3 (d, / = 16.0 Hz), 132.5 (d, 7 = 3.7 Hz), 131.8, 131.0, 129.5, 123.7 (d, 7 = 3.6 Hz), 120.8, 111.7, 110.0 (d, 7 = 1.0 Hz), 70.7 (d, 7 = 23.3 Hz), 55.8 (d, 7 = 0.8 Hz), 31.6 (d, 7 = 19.7 Hz); 27.7 (d, 7 = 14.3 Hz); ESI-MS: m/z 301 [M +H]⁺.

Example 11 : (5')-3-tert-butyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[if| [ 1 ,3]oxaphosphole oxide

(5')-3-tert-butyl-4-(2,6-diisopropoxyphenyl)-2,3-dihydrobenzo[if|[l,3]oxaphosphole oxide was prepared under a similar condition described in Example 3: 27% yield; 'HNMR (500 MHz, CDC1₃): δ = 7.43 (t, 7 = 7.8 Hz, 1H), 7.20 (t, 7 = 8.4 Hz, 1H), 6.84 (m, 2H), 6.56 (d, 7 = 8.4 Hz, 1H), 6.47 (d, 7 = 8.4 Hz, 1H), 4.47 (m, 3H), 4.31 (dd, 7 = 13.6, 10.5 Hz, 1H), 1.31 (d, 7 = 6.1 Hz, 3H), 1.22 (d, 7 = 6.0 Hz, 3H), 1.17 (d, 7 = 6.1 Hz, 6H), 0.92 (d, 7 = 15.9 Hz, 9H); ³¹PNMR (202 MHz, CDC1₃): δ= 61.7; ESI-MS: m/z 403 [M +H]⁺.

Example 12: (/?)-3-tert-butyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[if| [ 1 ,3]oxaphosphole

(/?)-3-tert-butyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[if|[l,3]oxaphosphole was prepared under a similar condition describled in Example 4; 95% yield; *HNMR (400 MHz, CD₂C1₂): δ= 7.25 (t, 7 = 7.9 Hz, 1H), 7.20 (t, / = 8.4 Hz, 1H), 6.81 (d, / = 8.4 Hz, 1H), 6.79 (m, 1H), 6.55 (t, / = 8.9 Hz, 2H), 4.71 (dd, J = 12.5, 1.6 Hz, 1H), 4.30-4.55 (m, 3H), 1.27 (d, / = 6.4 Hz, 3H), 1.25 (d, / = 6.6 Hz, 3H), 1.15 (d, / = 6.0 Hz, 3H), 1.10 (d, / = 6.0 Hz, 3H), 0.73 (d, / = 12.0 Hz); ³¹PNMR (162 MHz, CD₂C1₂): S= -6.0; ¹³CNMR (100 MHz, CD₂C1₂): S= 163.9, 157.1, 156.5, 139.9 (d, J = 17.8 Hz), 130.4, 129.2, 124.8 (d, / = 4.4 Hz), 121.7, 109.2, 106.9, 105.1, 71.4, 70.8 (d, J = 27.6 Hz), 69.8, 31.2 (d, / = 19.0 Hz), 27.2 (d, / = 14.7 Hz), 22.8 (d, / = 4.5 Hz), 22.7, 22.5, 22.4; ESI-MS: m/z 387 [M +H]⁺.

Experiment 13: 2-methyl-l-o-tolylnaphthalene (A typical example of Suzuki-Miyaura coupling catalyzed by a metal complex of a ligand according to the present invention as

To a mixture of 2-methylnaphthalen-l-ylboronic acid (0.15 g, 0.75 mmol, 1.5 equiv) and 1 -bromo-2-methylbenzene (86 mg, 0.5 mmol, 1.0 equiv),

tris(dibenzylideneacetone)dipalladium (9.16 mg, 0.01 m mol, 2 mol ), 3-ieri-butyl-4- phenyl-2,3-dihydrobenzo[if|[l,3]oxaphosphole (11 mg, 0.04 mmol, 8 mol ), and potassium phosphate (0.318 g, 1.5 mmol, 3 equiv) was charged dagassed toluene (4 mL). The mixture was stirred at 70 °C under nitrogen for 24 h, then quenched with water (4 mL). The organic phase was separated, washed with brine, dried over sodium sulfate, concentrated, and purified by column chromatography to provide pure desired product as oil (95 mg, 0.41 mmol, 82%). ESI-MS: m/z 233 [M +H]⁺

Experiment 14: 2'-phenyl-2,4,6-trimethylbiphenyl

To a mixture of biphenyl-2-ylboronic acid (0.15 g, 0.75 mmol, 1.5 equiv) and 2-bromo- 1,3,5-trimethylbenzene (100 mg, 0.5 mmol, 1.0 equiv),

tris(dibenzylideneacetone)dipalladium (0.46 mg, 0.0005 m mol, 0.1 mol %), 3-tert-butyl-4- (2,6-dimethoxyphenyl)-2,3-dihydrobenzo[if|[l,3]oxaphosphole (0.66 mg, 0.04 mmol, 0.4 mol %), and potassium phosphate (0.318 g, 1.5 mmol, 3 equiv) was charged dagassed toluene (4 mL). The mixture was stirred at 70 °C under nitrogen for 3 h, then quenched with water (4 mL). The organic phase was separated, washed with brine, dried over sodium sulfate, concentrated, and purified by column chromatography to provide pure desired product as oil (129 mg, 0.48 mmol, 95%). ESI-MS: m/z 273 [M +H]⁺.

Claims

CLAIMS:

R is (Ci-C6)-alkyl, CF₃, (C₃-Cio)-carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl, or ferrocenyl, wherein each such (C₃- Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 11- membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl, and CF₃; R¹, R², R³, R⁴, R⁵ are each independently selected from the group consisting of H, halo,

CF₃, -0(C₁-C₆)alkyl, (C₁-C₆)alkyl, (C₃-C₁₀)carbocyclyl, (5- to 11- membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl, -NRⁿR¹², - Si(Rⁿ)3 and -SR¹¹, wherein each such (C3-Cio)carbocyclyl, (5- to 11- membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to l l-membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl and CF₃; or any two adjacent instances of R¹, R², R³, R⁴, R⁵, taken together with the carbons to which they are bound, form a five- or six-membered substituted or unsubstituted aryl or heteroaryl ring; provided that at least one of R¹, R², R³, R⁴, R⁵ are OR¹¹; R⁶, R⁷, R⁸ are each independently selected from the group consisting of H, CF₃, -0(Ci- C6)alkyl, (Ci-C6)alkyl, (C3-Cio)carbocyclyl, (5- to 11 -membered)heterocarbocyclyl, (C6-Cio)aryl, (5 to 11 -membered)heteroaryl and -NRⁿR¹²; wherein each such (C3- Cio)carbocyclyl, (5- to l l-membered)heterocarbocyclyl, (C6-Cio)aryl or (5 to 11- membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C6)alkyl, and CF₃;

R⁹, R¹⁰ are each independently selected from the group consisting of H, (Ci-C6)alkyl, (C3-C6)cycloalkyl, (3- to 6-membered)heterocycloalkyl, (C6-Cio)aryl, (5- to 6- membered)heteroaryl, and -SiR⁵3 ; wherein each such (C3-C6)cycloalkyl, (3- to 6- membered)heterocycloalkyl, (C6-Cio)aryl or (5- to 6-membered)heteroaryl group is optionally substituted with 1 to 3 substituents independently selected from the group consisting of -0(Ci-C6)alkyl, (Ci-C₆)alkyl, and CF₃; and

2. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R is -(Ci-C₆)alkyl selected from -CH₃, -CH₂CH₃, -CH(CH₃)₂, -C(CH₃)₃, -C(CH₂CH₃)3, and -C(CH₂CH3)(CH₃)₂.

3. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R is -(C3-Cio)carbocyclyl selected from cyclopentyl, cyclohexyl, and 1- adamantyl.

4. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R is -(C6-Cio)aryl selected from phenyl, ortho-tolyl, para-tolyl, 3,5- dimethylphenyl, 3,5-di-i-butylphenyl, 3,5-di-CF₃-phenyl, ortho-CF₃-phenyl, ortho- anisyl, and naphthyl.

5. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R¹, R², R³, R⁴, R⁵ are each independently H, -CH₃, -CH₂CH₃, -CH(CH₃)₂, -C(CH₃)₃, -OCH₃, -OCH₂CH₃, -OCH(CH₃)₂, N(CH₃)₂, N(CH₂CH₃)₂, or SiMe₃.

6. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R⁶, R⁷, R⁸ are H.

7. A compound of formula (la), (lb), or a mixture thereof, in accordance with claim 1, wherein R⁹ and R¹⁰ are each independently H, -CH₃, -CH₂CH₃, -CH(CH₃)₂, -C(CH₃)₃, phenyl, ortho-tolyl, para-tolyl, 3,5-dimethylphenyl, 3,5-di-i-butylphenyl, 3,5-di-CF₃- phenyl, ortho-CF₃-phenyl, ortho-anisyl, 2,6-dimethoxyphenyl or naphthyl.

8. A phosphine lig thereof,

wherein:

R is -CH(CH₃)₂, -C(CH₃)₃ -C(CH₂CH₃)(CH₃)_2, cyclohexyl, 1-adamantyl, phenyl, ortho- tolyl, 3,5-xylyl, ortho-anisyl, or ferrocenyl; and

R¹, R², and R³ are independently H, -CH₃, -CH₂CH₃, -CH(CH₃)₂, -C(CH₃)₃, -OCH₃, -OCH₂CH_3, -OCH(CH₃)₂, OPh, N(CH₃)₂, N(CH₂CH₃)₂, SiMe₃, CF₃.

9. A phosphine ligand selected from the group consisting of:

(S) and (/?)-3-tert-butyl-4-phenyl-2,3-dihydrobenzo[if|[l ,3]oxaphosphole,

(5") and («)-2-(3-tert-butyl-2,3-dihydrobenzo[d] [l ,3]oxaphosphol-4-yl)-N,N- dimethylaniline,

(S) and (/?)-3-tert-butyl-4-o-tolyl-2,3-dihydrobenzo[d][l ,3]oxaphosphole,

(S) and (/?)-3-cyclohexyl-4-(2,6-diisopropoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole,

(S) and (R)-3- cyclohexyl-4-o-tolyl-2,3-dihydrobenzo[d][l ,3]oxaphosphole, and (S) and (R)-3- cyclohexyl-4-(2-phenoxyphenyl)-2,3- dihydrobenzo[d] [1 ,3]oxaphosphole.