ES433891A1 - Procedimiento para la preparacion de nuevas bencilaminas. - Google Patents

Procedimiento para la preparacion de nuevas bencilaminas.

Info

Publication number: ES433891A1
Authority: ES; Spain
Prior art keywords: general formula; radicals; radical; compound; represent
Prior art date: 1973-04-13
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

ES433891A

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.)

Boehringer Ingelheim Pharma GmbH and Co KG

Original Assignee

Dr Karl Thomae GmbH

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.)

1973-04-13

Filing date

1975-01-17

Publication date

1976-11-16

1973-04-13 Priority claimed from DE19732318636 external-priority patent/DE2318636B2/de

1974-01-23 Priority claimed from DE19742402989 external-priority patent/DE2402989C3/de

1974-03-20 Priority claimed from ES424432A external-priority patent/ES424432A1/es

1975-01-17 Application filed by Dr Karl Thomae GmbH filed Critical Dr Karl Thomae GmbH

1975-01-17 Priority to ES433891A priority Critical patent/ES433891A1/es

1976-11-16 Publication of ES433891A1 publication Critical patent/ES433891A1/es

Status Expired legal-status Critical Current

Links

150000003939 benzylamines Chemical class 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 6
-1 cyano, carbamoyl Chemical group 0.000 abstract 5
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 4
150000001875 compounds Chemical class 0.000 abstract 4
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 3
230000007062 hydrolysis Effects 0.000 abstract 3
238000006460 hydrolysis reaction Methods 0.000 abstract 3
230000001681 protective effect Effects 0.000 abstract 3
125000003277 amino group Chemical group 0.000 abstract 2
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
238000007327 hydrogenolysis reaction Methods 0.000 abstract 2
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
150000007522 mineralic acids Chemical class 0.000 abstract 2
229910052757 nitrogen Inorganic materials 0.000 abstract 2
125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
150000007524 organic acids Chemical class 0.000 abstract 2
150000003839 salts Chemical class 0.000 abstract 2
125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 abstract 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
239000002253 acid Substances 0.000 abstract 1
230000001476 alcoholic effect Effects 0.000 abstract 1
125000001931 aliphatic group Chemical group 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 abstract 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
229910052731 fluorine Inorganic materials 0.000 abstract 1
125000001153 fluoro group Chemical group F* 0.000 abstract 1
229960004011 methenamine Drugs 0.000 abstract 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Peptides Or Proteins (AREA)

ES433891A 1973-04-13 1975-01-17 Procedimiento para la preparacion de nuevas bencilaminas. Expired ES433891A1 (es)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
ES433891A ES433891A1 (es)	1973-04-13	1975-01-17	Procedimiento para la preparacion de nuevas bencilaminas.

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE19732318636 DE2318636B2 (de)	1973-04-13	1973-04-13	Neue benzylamine, sie enthaltende arzneimittel und verfahren zu ihrer herstellung
DE19742402989 DE2402989C3 (de)	1974-01-23	1974-01-23	Neue Benzylamine, sie enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
ES424432A ES424432A1 (es)	1973-04-13	1974-03-20	Procedimiento para la preparacion de nuevas bencilaminas.
ES433891A ES433891A1 (es)	1973-04-13	1975-01-17	Procedimiento para la preparacion de nuevas bencilaminas.

Publications (1)

Publication Number	Publication Date
ES433891A1 true ES433891A1 (es)	1976-11-16

Family

ID=27431668

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES433891A Expired ES433891A1 (es)	1973-04-13	1975-01-17	Procedimiento para la preparacion de nuevas bencilaminas.

Country Status (1)

Country	Link
ES (1)	ES433891A1 (es)

1975
- 1975-01-17 ES ES433891A patent/ES433891A1/es not_active Expired

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