ES446082A1 - Procedimiento para la obtencion de derivados de 1-pirazini- loxi-2-hidroxi-3-aminopropano. - Google Patents

Procedimiento para la obtencion de derivados de 1-pirazini- loxi-2-hidroxi-3-aminopropano.

Info

Publication number: ES446082A1
Authority: ES; Spain
Prior art keywords: carbon atoms; amino; case; alkyl; lower alkyl
Prior art date: 1973-02-20
Legal status (The legal status 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 status listed.): Expired

Application number

ES76446082A

Other languages

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

Original Assignee

Ciba Geigy AG

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.)

1973-02-20

Filing date

1976-03-16

Publication date

1977-10-01

1973-02-20 Priority claimed from CH244473A external-priority patent/CH584209A5/de

1974-01-08 Priority claimed from CH19374A external-priority patent/CH603657A5/xx

1976-03-16 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1977-10-01 Publication of ES446082A1 publication Critical patent/ES446082A1/es

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title abstract 2
125000004432 carbon atom Chemical group C* 0.000 abstract 23
125000000217 alkyl group Chemical group 0.000 abstract 21
125000002947 alkylene group Chemical group 0.000 abstract 10
125000003545 alkoxy group Chemical group 0.000 abstract 8
229910052736 halogen Inorganic materials 0.000 abstract 7
150000002367 halogens Chemical class 0.000 abstract 7
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
125000003342 alkenyl group Chemical group 0.000 abstract 3
125000003302 alkenyloxy group Chemical group 0.000 abstract 3
125000003282 alkyl amino group Chemical group 0.000 abstract 3
150000001875 compounds Chemical class 0.000 abstract 3
150000003839 salts Chemical class 0.000 abstract 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
125000004849 alkoxymethyl group Chemical group 0.000 abstract 2
229910052799 carbon Inorganic materials 0.000 abstract 2
125000004181 carboxyalkyl group Chemical group 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
QKXFPUNRUTVAIT-UHFFFAOYSA-N 1-amino-3-pyrazin-2-yloxypropan-2-ol Chemical class NCC(O)COC1=CN=CC=N1 QKXFPUNRUTVAIT-UHFFFAOYSA-N 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
125000005236 alkanoylamino group Chemical group 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
125000005189 alkyl hydroxy group Chemical group 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000004414 alkyl thio group Chemical group 0.000 abstract 1
125000004103 aminoalkyl group Chemical group 0.000 abstract 1
125000004429 atom Chemical group 0.000 abstract 1
102000012740 beta Adrenergic Receptors Human genes 0.000 abstract 1
108010079452 beta Adrenergic Receptors Proteins 0.000 abstract 1
125000005242 carbamoyl alkyl group Chemical group 0.000 abstract 1
-1 cyano, hydroxy Chemical group 0.000 abstract 1
125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
230000000694 effects Effects 0.000 abstract 1
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
239000000203 mixture Substances 0.000 abstract 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
230000003287 optical effect Effects 0.000 abstract 1
125000003884 phenylalkyl group Chemical group 0.000 abstract 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1

Landscapes

Plural Heterocyclic Compounds (AREA)

ES76446082A 1973-02-20 1976-03-16 Procedimiento para la obtencion de derivados de 1-pirazini- loxi-2-hidroxi-3-aminopropano. Expired ES446082A1 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH244473A CH584209A5 (en)	1973-02-20	1973-02-20	3-amino-2-hydroxypropoxy substd. diazines and pyridines - with beta-adrenergic blocking or stimulating activity
CH19374A CH603657A5 (es)	1973-02-08	1974-01-08

Publications (1)

Publication Number	Publication Date
ES446082A1 true ES446082A1 (es)	1977-10-01

Family

ID=25683828

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES76446082A Expired ES446082A1 (es)	1973-02-20	1976-03-16	Procedimiento para la obtencion de derivados de 1-pirazini- loxi-2-hidroxi-3-aminopropano.

Country Status (1)

Country	Link
ES (1)	ES446082A1 (es)

1976
- 1976-03-16 ES ES76446082A patent/ES446082A1/es not_active Expired

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