GB1183093A - Novel Indole Derivatives and a process for producing the same - Google Patents

Novel Indole Derivatives and a process for producing the same

Info

Publication number
GB1183093A
GB1183093A GB1216267A GB1216267A GB1183093A GB 1183093 A GB1183093 A GB 1183093A GB 1216267 A GB1216267 A GB 1216267A GB 1216267 A GB1216267 A GB 1216267A GB 1183093 A GB1183093 A GB 1183093A
Authority
GB
United Kingdom
Prior art keywords
alkoxy
halogen
alkyl
formula
substituted
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
GB1216267A
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of GB1183093A publication Critical patent/GB1183093A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56Ring systems containing three or more rings
    • C07D209/80[b, c]- or [b, d]-condensed
    • C07D209/82Carbazoles; Hydrogenated carbazoles
    • C07D209/88Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

1,183,093. Indole derivatives. SUMITOMO CHEMICAL CO. Ltd. 15 March, 1967 [16 March, 1966; 10 Jan., 1967], No. 12162/67. Heading C2C. Novel indole derivatives of the formula wherein R<SP>1</SP> is a C 1-3 alkyl-, C 1-3 alkoxy-, C 1-3 alkylthio- or halogen-substituted phenyl or naphthyl group or an unsubstituted naphthyl group, an unsubstituted or halogen- or C 1-3 alkyl-substituted 5- or 6-membered heterocyclic ring containing a nitrogen, oxygen or sulphur, or an unsubstituted or halogen-, phenyl-, phenoxy- or C 1-2 alkoxy-substituted C 2-10 alkyl or C 2-10 alkenyl group; R<SP>2</SP> is C 1-3 alkoxy; R<SP>3</SP> and R<SP>4</SP> are independently hydrogen, halogen, hydroxycarbonyl. C 1-3 alkoxycarbonyl, C 1-3 alkyl, C 2-3 alkenyl, or C 1-3 alkoxy; and Y is a saturated chain containing 3 or 4 members, which may all be carbon atoms or one nitrogen and the rest carbon, and acid addition salts of compounds of the above formula in which Y contains a nitrogen atom are prepared by reacting at elevated temperatures suitably substituted phenylhydrazines of the formula with cyclic ketones of the formula Therapeutic compositions, having antiphlogistic, analgesic, antifebric and sedative activities, contain the above novel compounds or acid addition salts thereof and inert non-toxic pharmaceutical diluents or carriers.
GB1216267A 1966-03-16 1967-03-15 Novel Indole Derivatives and a process for producing the same Expired GB1183093A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1664066 1966-03-16
JP205667 1967-01-10

Publications (1)

Publication Number Publication Date
GB1183093A true GB1183093A (en) 1970-03-04

Family

ID=26335367

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1216267A Expired GB1183093A (en) 1966-03-16 1967-03-15 Novel Indole Derivatives and a process for producing the same

Country Status (1)

Country Link
GB (1) GB1183093A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4006164A (en) * 1974-04-01 1977-02-01 Pfizer Inc. 4-Aryl-1,2,3,4-tetrahydropyrrolo[3,4-b]indoles

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4006164A (en) * 1974-04-01 1977-02-01 Pfizer Inc. 4-Aryl-1,2,3,4-tetrahydropyrrolo[3,4-b]indoles

Also Published As

Publication number Publication date
DE1695703B2 (en) 1975-11-20
DE1695703A1 (en) 1971-04-22

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee