ES342940A1 - Un procedimiento de producir derivados de piperidina. - Google Patents

Un procedimiento de producir derivados de piperidina.

Info

Publication number: ES342940A1
Authority: ES; Spain
Prior art keywords: alkyl; substituents; carry; halogen; group
Prior art date: 1966-07-13
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

ES342940A

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.)

Novo Terapeutisk Laboratorium AS

Original Assignee

Novo Terapeutisk Laboratorium AS

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.)

1966-07-13

Filing date

1967-07-12

Publication date

1968-08-01

1967-07-12 Application filed by Novo Terapeutisk Laboratorium AS filed Critical Novo Terapeutisk Laboratorium AS

1968-08-01 Publication of ES342940A1 publication Critical patent/ES342940A1/es

Status Expired legal-status Critical Current

Links

150000003053 piperidines Chemical class 0.000 title 1
125000000217 alkyl group Chemical group 0.000 abstract 6
150000002367 halogens Chemical group 0.000 abstract 4
-1 hydrocarbon radical Chemical class 0.000 abstract 4
239000001257 hydrogen Substances 0.000 abstract 4
229910052739 hydrogen Inorganic materials 0.000 abstract 4
125000003118 aryl group Chemical group 0.000 abstract 3
150000001875 compounds Chemical class 0.000 abstract 3
229910052736 halogen Chemical group 0.000 abstract 3
PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 abstract 2
VRJHQPZVIGNGMX-UHFFFAOYSA-N 4-piperidinone Chemical compound O=C1CCNCC1 VRJHQPZVIGNGMX-UHFFFAOYSA-N 0.000 abstract 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical group C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 2
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 2
125000000753 cycloalkyl group Chemical group 0.000 abstract 2
DIXBSCZRIZDQGC-UHFFFAOYSA-N diaziridine Chemical group C1NN1 DIXBSCZRIZDQGC-UHFFFAOYSA-N 0.000 abstract 2
150000002431 hydrogen Chemical class 0.000 abstract 2
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 abstract 2
125000001424 substituent group Chemical group 0.000 abstract 2
HUUPVABNAQUEJW-UHFFFAOYSA-N 1-methylpiperidin-4-one Chemical compound CN1CCC(=O)CC1 HUUPVABNAQUEJW-UHFFFAOYSA-N 0.000 abstract 1
239000004215 Carbon black (E152) Substances 0.000 abstract 1
239000005977 Ethylene Substances 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
125000002252 acyl group Chemical group 0.000 abstract 1
125000001931 aliphatic group Chemical group 0.000 abstract 1
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000000304 alkynyl group Chemical group 0.000 abstract 1
150000001412 amines Chemical class 0.000 abstract 1
229910021529 ammonia Inorganic materials 0.000 abstract 1
125000003710 aryl alkyl group Chemical group 0.000 abstract 1
125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
150000001602 bicycloalkyls Chemical group 0.000 abstract 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
150000002170 ethers Chemical class 0.000 abstract 1
125000005842 heteroatom Chemical group 0.000 abstract 1
229930195733 hydrocarbon Natural products 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
230000003993 interaction Effects 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
MRRXGLNCXPJBJU-UHFFFAOYSA-N piperidin-4-imine Chemical compound N=C1CCNCC1 MRRXGLNCXPJBJU-UHFFFAOYSA-N 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
230000001225 therapeutic effect Effects 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Hydrogenated Pyridines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

ES342940A 1966-07-13 1967-07-12 Un procedimiento de producir derivados de piperidina. Expired ES342940A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB31393/66A GB1187393A (en)	1966-07-13	1966-07-13	Improvements in or relating to Piperidine Compounds

Publications (1)

Publication Number	Publication Date
ES342940A1 true ES342940A1 (es)	1968-08-01

Family

ID=10322434

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES342940A Expired ES342940A1 (es)	1966-07-13	1967-07-12	Un procedimiento de producir derivados de piperidina.

Country Status (8)

Country	Link
AT (1)	AT268324B (es)
BE (1)	BE701293A (es)
DE (1)	DE1695565A1 (es)
ES (1)	ES342940A1 (es)
FR (2)	FR1562790A (es)
GB (1)	GB1187393A (es)
GR (1)	GR33975B (es)
NL (1)	NL6709754A (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS549888B2 (es) *	1973-03-12	1979-04-28
WO2013121334A2 (en) *	2012-02-17	2013-08-22	Cro Consulting Limited	Agents for treating neurodegenerative disorders

1966
- 1966-07-13 GB GB31393/66A patent/GB1187393A/en not_active Expired
1967
- 1967-07-05 GR GR670133975A patent/GR33975B/el unknown
- 1967-07-12 ES ES342940A patent/ES342940A1/es not_active Expired
- 1967-07-12 BE BE701293D patent/BE701293A/xx unknown
- 1967-07-12 DE DE19671695565 patent/DE1695565A1/de active Pending
- 1967-07-13 AT AT657867A patent/AT268324B/de active
- 1967-07-13 NL NL6709754A patent/NL6709754A/xx unknown
- 1967-07-13 FR FR1562790D patent/FR1562790A/fr not_active Expired
- 1967-10-13 FR FR124432A patent/FR7176M/fr not_active Expired

Also Published As

Publication number	Publication date
NL6709754A (es)	1968-01-15
FR7176M (es)	1969-08-11
DE1695565A1 (de)	1970-07-16
FR1562790A (es)	1969-04-11
AT268324B (de)	1969-02-10
GR33975B (el)	1968-02-29
GB1187393A (en)	1970-04-08
BE701293A (es)	1968-01-12

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