DD251135A5 - Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methyl-glycyl-)amin-derivaten - Google Patents

Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methyl-glycyl-)amin-derivaten Download PDF

Info

Publication number: DD251135A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; alkyl; items; mmol; radical
Prior art date: 1984-12-26

Application number

DD85285097A

Other languages

German (de)

English (en)

Inventor

Herve Bres

Serge Veracini

Original Assignee

��`��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-12-26

Filing date

1985-12-23

Publication date

1987-11-04

1985-12-23 Application filed by ��`��@��k�� filed Critical ��`��@��k��

1987-11-04 Publication of DD251135A5 publication Critical patent/DD251135A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 17
-1 PHOSPHONO-METHYL-GLYCYL- Chemical class 0.000 title abstract description 9
150000001412 amines Chemical class 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 6
238000002360 preparation method Methods 0.000 claims abstract description 6
125000000217 alkyl group Chemical group 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 13
125000003118 aryl group Chemical group 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
239000002904 solvent Substances 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
239000002253 acid Substances 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
239000000376 reactant Substances 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
229930195733 hydrocarbon Natural products 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
239000003513 alkali Substances 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000005599 alkyl carboxylate group Chemical group 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
150000002825 nitriles Chemical group 0.000 claims description 2
239000002798 polar solvent Substances 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
229910001854 alkali hydroxide Inorganic materials 0.000 claims 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
150000008282 halocarbons Chemical class 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
125000001302 tertiary amino group Chemical group 0.000 claims 1
239000004009 herbicide Substances 0.000 abstract description 4
239000000543 intermediate Substances 0.000 abstract description 2
239000000126 substance Substances 0.000 abstract 1
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 30
239000000047 product Substances 0.000 description 23
OJTRKMSUJCHVMW-UHFFFAOYSA-N 2-chloro-n-methyl-n-methylsulfonylacetamide Chemical compound CS(=O)(=O)N(C)C(=O)CCl OJTRKMSUJCHVMW-UHFFFAOYSA-N 0.000 description 17
239000000243 solution Substances 0.000 description 15
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
238000004587 chromatography analysis Methods 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 11
239000000203 mixture Substances 0.000 description 11
238000010438 heat treatment Methods 0.000 description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 8
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XNZGZECZGFXBJP-UHFFFAOYSA-N P(O)(O)=O.C(C)C(NCC1=CC=CC=C1)CC Chemical compound P(O)(O)=O.C(C)C(NCC1=CC=CC=C1)CC XNZGZECZGFXBJP-UHFFFAOYSA-N 0.000 description 3
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
AEJXRXSZGRQHMG-UHFFFAOYSA-N P(O)(O)=O.C1(=CC=CC=C1)C(NCC1=CC=CC=C1)C1=CC=CC=C1 Chemical compound P(O)(O)=O.C1(=CC=CC=C1)C(NCC1=CC=CC=C1)C1=CC=CC=C1 AEJXRXSZGRQHMG-UHFFFAOYSA-N 0.000 description 2
239000007983 Tris buffer Substances 0.000 description 2
QVERGTKSWSYQEY-UHFFFAOYSA-N [[2-oxo-2-(sulfonylamino)ethyl]amino]methylphosphonic acid Chemical class OP(O)(=O)CNCC(=O)N=S(=O)=O QVERGTKSWSYQEY-UHFFFAOYSA-N 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000010992 reflux Methods 0.000 description 2
OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical class C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
VJPHWIBYCFXNDG-UHFFFAOYSA-N P(O)(O)=O.C(C)(C)C(NCC1=CC=CC=C1)C(C)C Chemical compound P(O)(O)=O.C(C)(C)C(NCC1=CC=CC=C1)C(C)C VJPHWIBYCFXNDG-UHFFFAOYSA-N 0.000 description 1
CQNLIGPPHZDRJV-UHFFFAOYSA-N P(O)(O)=O.C(C1=CC=CC=C1)C(NCC1=CC=CC=C1)CC1=CC=CC=C1 Chemical compound P(O)(O)=O.C(C1=CC=CC=C1)C(NCC1=CC=CC=C1)CC1=CC=CC=C1 CQNLIGPPHZDRJV-UHFFFAOYSA-N 0.000 description 1
CEVYGKPEZSUGDC-UHFFFAOYSA-N P(O)(O)=O.CC(NCC1=CC=CC=C1)C Chemical compound P(O)(O)=O.CC(NCC1=CC=CC=C1)C CEVYGKPEZSUGDC-UHFFFAOYSA-N 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
URAZVWXGWMBUGJ-UHFFFAOYSA-N di(propan-2-yl)azanium;chloride Chemical compound [Cl-].CC(C)[NH2+]C(C)C URAZVWXGWMBUGJ-UHFFFAOYSA-N 0.000 description 1
229940043279 diisopropylamine Drugs 0.000 description 1
238000001914 filtration Methods 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
LEWADWGCENKZJX-UHFFFAOYSA-N n-(diethoxyphosphorylmethyl)-1-phenylmethanamine Chemical compound CCOP(=O)(OCC)CNCC1=CC=CC=C1 LEWADWGCENKZJX-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60Q—ARRANGEMENT OF SIGNALLING OR LIGHTING DEVICES, THE MOUNTING OR SUPPORTING THEREOF OR CIRCUITS THEREFOR, FOR VEHICLES IN GENERAL
- B60Q1/00—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor
- B60Q1/0064—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor with provision for maintenance, e.g. changing the light bulb
- B60Q1/007—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor with provision for maintenance, e.g. changing the light bulb via a removable cap
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21S—NON-PORTABLE LIGHTING DEVICES; SYSTEMS THEREOF; VEHICLE LIGHTING DEVICES SPECIALLY ADAPTED FOR VEHICLE EXTERIORS
- F21S41/00—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps
- F21S41/10—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps characterised by the light source
- F21S41/19—Attachment of light sources or lamp holders
- F21S41/196—Wire spring attachments
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21S—NON-PORTABLE LIGHTING DEVICES; SYSTEMS THEREOF; VEHICLE LIGHTING DEVICES SPECIALLY ADAPTED FOR VEHICLE EXTERIORS
- F21S41/00—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps
- F21S41/10—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps characterised by the light source
- F21S41/19—Attachment of light sources or lamp holders
- F21S41/198—Snap-fit attachments
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21S—NON-PORTABLE LIGHTING DEVICES; SYSTEMS THEREOF; VEHICLE LIGHTING DEVICES SPECIALLY ADAPTED FOR VEHICLE EXTERIORS
- F21S41/00—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps
- F21S41/50—Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps characterised by aesthetic components not otherwise provided for, e.g. decorative trim, partition walls or covers
- F21S41/55—Attachment thereof

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
General Engineering & Computer Science (AREA)
Molecular Biology (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Mechanical Engineering (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Fertilizers (AREA)
Saccharide Compounds (AREA)
Cephalosporin Compounds (AREA)

DD85285097A 1984-12-26 1985-12-23 Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methyl-glycyl-)amin-derivaten DD251135A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR8420151A FR2575161B1 (fr)	1984-12-26	1984-12-26	Preparation d'intermediaires phosphores pour usages herbicides

Publications (1)

Publication Number	Publication Date
DD251135A5 true DD251135A5 (de)	1987-11-04

Family

ID=9311173

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85285097A DD251135A5 (de)	1984-12-26	1985-12-23	Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methyl-glycyl-)amin-derivaten

Country Status (19)

Country	Link
EP (1)	EP0189725B1 (da)
JP (1)	JPS61158991A (da)
KR (1)	KR930007996B1 (da)
CN (1)	CN85109729A (da)
AT (1)	ATE41153T1 (da)
AU (1)	AU573410B2 (da)
BR (1)	BR8506478A (da)
CA (1)	CA1244461A (da)
DD (1)	DD251135A5 (da)
DE (1)	DE3568579D1 (da)
DK (1)	DK603585A (da)
ES (1)	ES8706161A1 (da)
FI (1)	FI855066A7 (da)
FR (1)	FR2575161B1 (da)
HU (1)	HU199855B (da)
IL (1)	IL77445A (da)
NO (1)	NO855244L (da)
PT (1)	PT81756B (da)
ZA (1)	ZA859769B (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES534413A0 (es) *	1983-07-27	1986-01-01	Rhone Poulenc Agrochimie	Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico
FR2576024B1 (fr) *	1985-01-14	1988-01-08	Rhone Poulenc Agrochimie	Herbicides de type n - (phosphonomethylglycyl) sulfonylamines
FR2579210B1 (fr) *	1985-03-21	1987-09-11	Rhone Poulenc Agrochimie	Preparation d'herbicides a groupe phosphonates et d'intermediaires a partir de benzoxazines
FR2608609B1 (fr) *	1986-12-18	1989-06-02	Rhone Poulenc Agrochimie	Preparation d'intermediaires phosphores pour usage herbicide

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4414158A (en) *	1980-04-29	1983-11-08	Ciba-Geigy Corporation	Phosphonomethylglycylhydroxamic acid and novel herbicidally active salts thereof

1984
- 1984-12-26 FR FR8420151A patent/FR2575161B1/fr not_active Expired
1985
- 1985-12-18 FI FI855066A patent/FI855066A7/fi not_active Application Discontinuation
- 1985-12-20 AU AU51519/85A patent/AU573410B2/en not_active Ceased
- 1985-12-20 ZA ZA859769A patent/ZA859769B/xx unknown
- 1985-12-20 CA CA000498283A patent/CA1244461A/en not_active Expired
- 1985-12-23 DK DK603585A patent/DK603585A/da not_active Application Discontinuation
- 1985-12-23 DD DD85285097A patent/DD251135A5/de unknown
- 1985-12-23 NO NO855244A patent/NO855244L/no unknown
- 1985-12-23 HU HU854956A patent/HU199855B/hu unknown
- 1985-12-23 PT PT81756A patent/PT81756B/pt not_active IP Right Cessation
- 1985-12-24 DE DE8585420242T patent/DE3568579D1/de not_active Expired
- 1985-12-24 EP EP85420242A patent/EP0189725B1/fr not_active Expired
- 1985-12-24 AT AT85420242T patent/ATE41153T1/de not_active IP Right Cessation
- 1985-12-24 IL IL77445A patent/IL77445A/xx unknown
- 1985-12-24 BR BR8506478A patent/BR8506478A/pt unknown
- 1985-12-24 JP JP60291796A patent/JPS61158991A/ja active Pending
- 1985-12-25 CN CN198585109729A patent/CN85109729A/zh active Pending
- 1985-12-26 KR KR1019850009835A patent/KR930007996B1/ko not_active Expired - Lifetime
- 1985-12-26 ES ES550424A patent/ES8706161A1/es not_active Expired

Also Published As

Publication number	Publication date
FI855066A0 (fi)	1985-12-18
AU573410B2 (en)	1988-06-09
CA1244461A (en)	1988-11-08
HU199855B (en)	1990-03-28
EP0189725B1 (fr)	1989-03-08
ZA859769B (en)	1986-09-24
PT81756B (pt)	1988-04-21
DE3568579D1 (en)	1989-04-13
PT81756A (fr)	1986-01-02
FR2575161B1 (fr)	1989-03-31
FR2575161A1 (fr)	1986-06-27
EP0189725A1 (fr)	1986-08-06
ES550424A0 (es)	1987-06-01
JPS61158991A (ja)	1986-07-18
KR860004902A (ko)	1986-07-16
AU5151985A (en)	1986-07-03
DK603585A (da)	1986-06-27
ATE41153T1 (de)	1989-03-15
NO855244L (no)	1986-06-27
DK603585D0 (da)	1985-12-23
BR8506478A (pt)	1986-09-02
IL77445A (en)	1989-09-10
ES8706161A1 (es)	1987-06-01
CN85109729A (zh)	1986-07-09
HUT39751A (en)	1986-10-29
FI855066L (fi)	1986-06-27
KR930007996B1 (ko)	1993-08-25
FI855066A7 (fi)	1986-06-27

Publication	Publication Date	Title
DE1146486B (de)	1963-04-04	Verfahren zur Herstellung von O, O-Dialkyl-dithiophosphorylfettsaeure-amiden
DE2650434C2 (da)	1989-01-26
DD251135A5 (de)	1987-11-04	Verfahren zur herstellung von n-sulfonyl-n-(phosphono-methyl-glycyl-)amin-derivaten
EP0000924B1 (de)	1981-04-29	Heterocyclische Phenyläther und Verfahren zu ihrer Herstellung
EP0245690A1 (de)	1987-11-19	Verfahren zur Herstellung von 4-Hydroxy-chinolin-3-carbon-säuren
DD239591A5 (de)	1986-10-01	Verfahren zur herstellung von 2,4-dichlor-5-fluor-benzoesaeure
EP0062608B1 (de)	1985-07-10	4-Halogenstilbenderivate und Verfahren zu deren Herstellung
DE4026026A1 (de)	1992-02-20	Acylaminomethyl-phosphinsaeuren und verfahren zur herstellung von acylaminomethanphosphonsaeuren und acylaminomethyl-phosphinsaeuren
DE3203538C2 (da)	1993-06-17
WO1992003449A1 (de)	1992-03-05	Verfahren zur herstellung von aminomethanphosphonsäure und aminomethyl-phosphinsäuren
DE2814330B2 (de)	1980-07-31	Verfahren zur Herstellung von 2,6-Dichlorpyridin-Derivaten
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