Verfahren zur Herstellung von tricyclischen Verbindungen

1,236,712. Dibenzocycloheptene derivatives. F. HOFFMANN-LA ROCHE & CO. A.G. 13 March, 1969 [20 March, 1968], No. 13202/69. Heading C2C. The invention comprises compounds of the Formula (VII) wherein R is Cl or F, R 1 and R 2 each denotes H, Cl or F, R 3 denotes H, C 1-7 alkanoyl or benzoyl, whic...

Full description

Saved in:
Bibliographic Details
Main Authors SPIEGELBERG,HANS,DR, KYBURZ,EMILIO,DR
Format Patent
LanguageGerman
Published 15.08.1973
Edition1
Subjects
Online AccessGet full text

Cover

Loading…
Abstract 1,236,712. Dibenzocycloheptene derivatives. F. HOFFMANN-LA ROCHE & CO. A.G. 13 March, 1969 [20 March, 1968], No. 13202/69. Heading C2C. The invention comprises compounds of the Formula (VII) wherein R is Cl or F, R 1 and R 2 each denotes H, Cl or F, R 3 denotes H, C 1-7 alkanoyl or benzoyl, which may be substituted, and X is the ethylene or vinylene group which can be substituted by Cl or Br and the dotted line can be hydrogenated, isomers thereof and acid addition salts; and compounds of the Formula (III) in which one of the symbols Y 1 and Y 2 denotes H and the other OH, and acid addition salts thereof. Compounds of Formula (VII) in which R 3 is H can be obtained by (a) oxidizing a compound of the Formula (II) (b) dehydrating a compound of the Formula (III), (c) treating with methylhydroxylamine a compound of one of the formulµ where Z denotes halogen or a substituted sulphonyloxy residue and A is the anion of an acid, or (d) saponifying a compound of Formula (VII) in which R 3 is a C 1-7 alkanoyl or benzoyl group, then, if desired, in optional sequence, isomers are isolated from an isomeric mixture, and the resulting base is converted to an acid addition salt. Compounds VII in which R 3 is C 1-7 alkanoyl or benzoyl, can be obtained, for example, by treating (II) with benzoyl peroxide, acetyl peroxide or acetyl benzoyl peroxide. Preparation of the following intermediates is also described (where DDCH denotes 10,11- dihydro - 5H - dibenzo[a,d]cycloheptene). 1-Chloro-DDCH-5-one is reacted with 1-chloro- 3-methoxypropane to yield 1-chloro-5-(3-methoxypropyl)-5-hydroxy DDCH which is refluxed with methanolic HCl forming 1-chloro- 5-(3-methoxypropylidene)-DDCH; the latter is reacted with BCl 3 to give 1-chloro-5-(3-chloropropylidene)-DDCH, which is reacted with methylamine to form 1-chloro-5-(3-methylaminopropylidene) - DDCH. 1 - Chloro-DDCH- 5-one is reacted with 3-dimethylamino-propylchloride giving 1 - chloro - 5 - hydroxy - 5 - (3- dimethylaminopropyl)-DDCH, which is then reacted with cyanogen bromide to form 1- chloro - 5 - (3 - N - cyano - N - methyl - aminopropyl)-DDCH; the latter is refluxed with cone. HCl to give 1.chloro.5.(3.methylamino. propyl)-DDCH. Pharmaceutical compositions having antidepressant activity comprise compounds of Formula (VII) in which R 3 is hydrogen, in association with a compatible pharmaceutical carrier, in forms suitable for enteral or parenteral administration.
AbstractList 1,236,712. Dibenzocycloheptene derivatives. F. HOFFMANN-LA ROCHE & CO. A.G. 13 March, 1969 [20 March, 1968], No. 13202/69. Heading C2C. The invention comprises compounds of the Formula (VII) wherein R is Cl or F, R 1 and R 2 each denotes H, Cl or F, R 3 denotes H, C 1-7 alkanoyl or benzoyl, which may be substituted, and X is the ethylene or vinylene group which can be substituted by Cl or Br and the dotted line can be hydrogenated, isomers thereof and acid addition salts; and compounds of the Formula (III) in which one of the symbols Y 1 and Y 2 denotes H and the other OH, and acid addition salts thereof. Compounds of Formula (VII) in which R 3 is H can be obtained by (a) oxidizing a compound of the Formula (II) (b) dehydrating a compound of the Formula (III), (c) treating with methylhydroxylamine a compound of one of the formulµ where Z denotes halogen or a substituted sulphonyloxy residue and A is the anion of an acid, or (d) saponifying a compound of Formula (VII) in which R 3 is a C 1-7 alkanoyl or benzoyl group, then, if desired, in optional sequence, isomers are isolated from an isomeric mixture, and the resulting base is converted to an acid addition salt. Compounds VII in which R 3 is C 1-7 alkanoyl or benzoyl, can be obtained, for example, by treating (II) with benzoyl peroxide, acetyl peroxide or acetyl benzoyl peroxide. Preparation of the following intermediates is also described (where DDCH denotes 10,11- dihydro - 5H - dibenzo[a,d]cycloheptene). 1-Chloro-DDCH-5-one is reacted with 1-chloro- 3-methoxypropane to yield 1-chloro-5-(3-methoxypropyl)-5-hydroxy DDCH which is refluxed with methanolic HCl forming 1-chloro- 5-(3-methoxypropylidene)-DDCH; the latter is reacted with BCl 3 to give 1-chloro-5-(3-chloropropylidene)-DDCH, which is reacted with methylamine to form 1-chloro-5-(3-methylaminopropylidene) - DDCH. 1 - Chloro-DDCH- 5-one is reacted with 3-dimethylamino-propylchloride giving 1 - chloro - 5 - hydroxy - 5 - (3- dimethylaminopropyl)-DDCH, which is then reacted with cyanogen bromide to form 1- chloro - 5 - (3 - N - cyano - N - methyl - aminopropyl)-DDCH; the latter is refluxed with cone. HCl to give 1.chloro.5.(3.methylamino. propyl)-DDCH. Pharmaceutical compositions having antidepressant activity comprise compounds of Formula (VII) in which R 3 is hydrogen, in association with a compatible pharmaceutical carrier, in forms suitable for enteral or parenteral administration.
Author SPIEGELBERG,HANS,DR
KYBURZ,EMILIO,DR
Author_xml – fullname: SPIEGELBERG,HANS,DR
– fullname: KYBURZ,EMILIO,DR
BookMark eNrjYmDJy89L5WSwCEstSkvMKErNU6gqLVLwSC0qLknNySnNS1coy89TKCnKTK5MzsksTs4AqgCqTcrMSwFKpubxMLCmJeYUp_JCaW4GOTfXEGcP3dSC_PjU4oLE5NS81JJ4Zw9TEwMjIyNHY4IKAEBKL2Y
ContentType Patent
DBID EVB
DatabaseName esp@cenet
DatabaseTitleList
Database_xml – sequence: 1
  dbid: EVB
  name: esp@cenet
  url: http://worldwide.espacenet.com/singleLineSearch?locale=en_EP
  sourceTypes: Open Access Repository
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Chemistry
Sciences
Edition 1
ExternalDocumentID CH540222A
GroupedDBID EVB
ID FETCH-epo_espacenet_CH540222A3
IEDL.DBID EVB
IngestDate Fri Jul 19 13:56:04 EDT 2024
IsOpenAccess true
IsPeerReviewed false
IsScholarly false
Language German
LinkModel DirectLink
MergedId FETCHMERGED-epo_espacenet_CH540222A3
Notes Application Number: CH19680004203
OpenAccessLink https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19730815&DB=EPODOC&CC=CH&NR=540222A
ParticipantIDs epo_espacenet_CH540222A
PublicationCentury 1900
PublicationDate 19730815
PublicationDateYYYYMMDD 1973-08-15
PublicationDate_xml – month: 08
  year: 1973
  text: 19730815
  day: 15
PublicationDecade 1970
PublicationYear 1973
RelatedCompanies F. HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT
RelatedCompanies_xml – name: F. HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT
Score 2.3258011
Snippet 1,236,712. Dibenzocycloheptene derivatives. F. HOFFMANN-LA ROCHE & CO. A.G. 13 March, 1969 [20 March, 1968], No. 13202/69. Heading C2C. The invention comprises...
SourceID epo
SourceType Open Access Repository
SubjectTerms AIR-CONDITIONING, AIR-HUMIDIFICATION, VENTILATION, USE OF AIRCURRENTS FOR SCREENING
BLASTING
HEATING
LIGHTING
MECHANICAL ENGINEERING
RANGES
VENTILATING
WEAPONS
Title Verfahren zur Herstellung von tricyclischen Verbindungen
URI https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19730815&DB=EPODOC&locale=&CC=CH&NR=540222A
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV3dS8MwED_mFH3U-f0x-iB9K1L6FR-KuHSlCG5D5tjbSJtEBqUdXavoX-8ldurL3kISQhJyufvl7ncBuLVZwAhzlMufBZabptIiUhGYs5Rw5jr-PdMBsiM_eXWf5t68A28bLozOE_qhkyOiRGUo77W-r1d_j1iRjq1c36VLrCof4mkYmfyHLobHldieGQ3C4WQcjalJaUgTc_QSomGCmvBxB3aVDa2S7A9nA0VJWf3XJ_Eh7E1wqKI-gg4XPTigm2_XerD_3Hq7sdgK3voYyExUkqnQOOOrqYxEGW0iz1FSjfeyMFSa_c8sXyJUxR7YF_EubxRt6gT68XBKEwunsPhd7IIm7VSdU-gWZSHOwZCB5zvCd7OME9fJPBbYUghmCwRf3PblBZxtGeRya8uVQqjqNQFBpHcN3bpqxA3q1zrt6735BhrFgZ0
link.rule.ids 230,309,786,891,25594,76906
linkProvider European Patent Office
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV1LT8MwDLbGQIwbjPdj9IB6q1DVJ4cKsXRVga2bUJl2m9I0RZOqdupaEPx6nNIBl92iJIocK47t2J8DcKNSi9pUEyF_ail6FCWKnQgAM4vsmOqaeUfrBNnA9F_1p5kxa8HbGgtT1wn9qIsjokQxlPeyvq-Xf49Ybp1bubqNFtiV33uh48rxD1wMj6utGrLbdwaTsTsmMiEO8eXgxUHDBDXhwxZsW6I0r7Cbpn0BSVn-1yfePuxMcKmsPIBWzLvQIetv17qwO2qi3dhsBG91CPaUFwkVqXHSV1VIvjDaeJqipErveSaJMvufLF2gq4ozcC76u3ElYFNH0PMGIfEVJGH-u9k58RtStWNoZ3nGT0FKLMPUuKkzFtu6xgxqqQnnVOXofMWqmZzByYZFzjeOXEPHD0fD-fAxeL6APcE78VSqGpfQLouKX6GuLaNezadvVDyEmA
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Apatent&rft.title=Verfahren+zur+Herstellung+von+tricyclischen+Verbindungen&rft.inventor=SPIEGELBERG%2CHANS%2CDR&rft.inventor=KYBURZ%2CEMILIO%2CDR&rft.date=1973-08-15&rft.externalDBID=A&rft.externalDocID=CH540222A