GB1025044A - N-substituted amides and the manufacture thereof - Google Patents

N-substituted amides and the manufacture thereof

Info

Publication number
GB1025044A
GB1025044A GB2729164A GB2729164A GB1025044A GB 1025044 A GB1025044 A GB 1025044A GB 2729164 A GB2729164 A GB 2729164A GB 2729164 A GB2729164 A GB 2729164A GB 1025044 A GB1025044 A GB 1025044A
Authority
GB
United Kingdom
Prior art keywords
group
amino
formula
alkoxy
benzylamino
Prior art date
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
GB2729164A
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche 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.)
Filing date
Publication date
Priority claimed from US292768A external-priority patent/US3282949A/en
Priority claimed from US292749A external-priority patent/US3270026A/en
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of GB1025044A publication Critical patent/GB1025044A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of formula <FORM:1025044/C2/1> wherein R1 is a hydrogen or halogen atom or a nitro, amino, C1- 7 alkylamino, di-(C1- 7 alkyl)-amino, benzylamino, halobenzylamino, or (C1- 7 alkoxy)-benzylamino group, or a group R5CH=N-, wherein R5 is a halophenyl or (C1- 7 alkoxy)-phenyl group, R2 and R3 are C1- 7 alkyl groups, and n is 1, 2 or 3, pharmaceutically acceptable acid addition salts thereof, and their preparation by reaction of a compound of formula <FORM:1025044/C2/2> with a compound of the formula <FORM:1025044/C2/3> wherein R10 has one of the values of R1 other than an amino or substituted imino group, and, if desired, reducing a nitro group to an amino group and converting this to a substituted amino-group R1, for example by conversion to a Schiff's base, followed by reduction. The compounds of the invention, other than where R1 is a substituted imino-group, have hypotensive and analgesic activity and may be used in pharmaceutical compositions in combination with a carrier, for example in forms suitable for oral, parenteral or rectal administration, such as tablets, capsules, dragees, ampoules, solutions, emulsions, suspensions and suppositories.
GB2729164A 1963-07-03 1964-07-02 N-substituted amides and the manufacture thereof Expired GB1025044A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US292768A US3282949A (en) 1963-07-03 1963-07-03 Substituted lower fatty acid amides and processes
US292749A US3270026A (en) 1963-07-03 1963-07-03 Substituted benzamidotetrahydro-pyridines and processes

Publications (1)

Publication Number Publication Date
GB1025044A true GB1025044A (en) 1966-04-06

Family

ID=26967538

Family Applications (2)

Application Number Title Priority Date Filing Date
GB2729064A Expired GB1018807A (en) 1963-07-03 1964-07-02 Novel tetrahydro-pyridine derivatives and the manufacture thereof
GB2729164A Expired GB1025044A (en) 1963-07-03 1964-07-02 N-substituted amides and the manufacture thereof

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB2729064A Expired GB1018807A (en) 1963-07-03 1964-07-02 Novel tetrahydro-pyridine derivatives and the manufacture thereof

Country Status (2)

Country Link
GB (2) GB1018807A (en)
NL (1) NL6407463A (en)

Also Published As

Publication number Publication date
NL6407463A (en) 1965-01-04
GB1018807A (en) 1966-02-02

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