GB1456161A - Diazepine derivatives - Google Patents

Diazepine derivatives

Info

Publication number
GB1456161A
GB1456161A GB568374A GB568374A GB1456161A GB 1456161 A GB1456161 A GB 1456161A GB 568374 A GB568374 A GB 568374A GB 568374 A GB568374 A GB 568374A GB 1456161 A GB1456161 A GB 1456161A
Authority
GB
United Kingdom
Prior art keywords
alkyl
compound
hydroxyalkyl
alkylcarbonyloxyalkyl
formula
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
GB568374A
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
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of GB1456161A publication Critical patent/GB1456161A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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 ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • C07D333/36Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14Ortho-condensed systems

Abstract

1456161 Thienotriazolodiazepines F HOFFMANN-LA ROCHE & CO AG 7 Feb 1974 [8 Feb 1973] 05683/74 Heading C2C Compounds of the general formula (R 1 = halogen, NO 2 , NH 2 , alkanoyl; R 2 = pyridyl or thienyl optionally substituted adjacent to linking position, phenyl, o-trifluoromethylphenyl, o - halophenyl, o,o<SP>1</SP> - dihalophenyl, o - nitrophenyl; R 3 = H, OH, alkoxycarbonyl, alkanoyloxy; R 4 = H, alkyl, alkanoyl, hydroxyalkyl, mercaptoalkyl, alkoxycarbonyl, aminocarbonyl, haloalkyl, alkoxyalkyl, alkylthioalkyl, aralkoxyalkyl, cyanoalkyl, alkoxycarbonylalkyl, alkoxycarbonylaminoalkyl, alkylcarbonyloxyalkyl, aminocarbonyloxyalkyl, dialkylaminocarbonyloxyalkyl, CN, alkyl NR 5 R 6 , COO alkyl NR 5 R 6 , CONH alkyl NR 5 R 6 ; R 5,6 = H, alkyl, hydroxyalkyl or NR 5 R 6 = monocyclic saturated 5-6 membered ring optionally containing an oxygen or further nitrogen atom; n = 0,1) and their acid addition salts are prepared by (a) cyclizing a compound of the formula (b) -n = O- cyclising a compound of the formula (c) -R 1 = halogen or NO 2 - halogenating or nitrating the corresponding 2-unsubstituted compound, (d) -R 4 = alkanoyloxidizing the corresponding 9-(α-hydroxyalkyl) compound, (e) -R 4 = alkylcarbonyloxyalkyl or aminocarbonyloxyalkylesterifying the corresponding alcohol, (f) -R 4 = alkoxyalkyl, aralkoxyalkyl, alkylthioalkyl or alkyl NR 5 R 6 - reacting a corresponding 9-A. alkyl compound with BR (one of A,B = OH, SH or NHR 5 and the other = leaving atom or group; R = alkyl or (one of A,B = OH) aralkyl, or (B = NHR 5 )H or hydroxyalkyl, or NRR 5 = monocyclic saturated 5-6 membered ring optionally containing an oxygen or further nitrogen atom), (g) -R 4 = alkylcarbonyloxyalkyl or dialkylaminocarbonyloxyalkyl-reacting the corresponding alcohol with a reactive derivative of the appropriate alkanoic or dialkylcarbamic acid, (h) -R 4 = alkoxycarbonylaminoalkylreacting a corresponding 9-K alkyl compound with L.COO- alkyl (one of K,L = NH 2 and the other = leaving atom or group) or (i) -R 4 = primary hydroxyalkylreducing a corresponding 9-alkoxy carbonyl or alkoxycarbonylalkyl compound, optionally followed by salt formation. The preparation of thienodiagepines of the formulµ and 2-amino, chloroacetamido and aminoacetamido-3-thienyl 2<SP>1</SP>-pyridyl ketone is described. The above compounds are anticonvulsants, sedatives, muscle relaxants, tranquilizerx and anxiolytics and may be administered in the form of pharmacetuical preparations containing them in association with a carrier.
GB568374A 1973-02-08 1974-02-07 Diazepine derivatives Expired GB1456161A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH179973A CH584223A5 (en) 1973-02-08 1973-02-08

Publications (1)

Publication Number Publication Date
GB1456161A true GB1456161A (en) 1976-11-17

Family

ID=4218866

Family Applications (2)

Application Number Title Priority Date Filing Date
GB539676A Expired GB1456162A (en) 1973-02-08 1974-02-07 Thienodiazepine derivatives
GB568374A Expired GB1456161A (en) 1973-02-08 1974-02-07 Diazepine derivatives

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB539676A Expired GB1456162A (en) 1973-02-08 1974-02-07 Thienodiazepine derivatives

Country Status (24)

Country Link
JP (1) JPS5833234B2 (en)
AR (2) AR203188A1 (en)
AT (1) AT343118B (en)
BE (1) BE810705A (en)
CA (1) CA1049009A (en)
CH (1) CH584223A5 (en)
DD (1) DD112454A5 (en)
DE (1) DE2405682C3 (en)
DK (1) DK137679B (en)
FI (1) FI58129C (en)
FR (1) FR2217007B1 (en)
GB (2) GB1456162A (en)
HU (2) HU170423B (en)
IE (1) IE38883B1 (en)
IL (1) IL44095A (en)
LU (1) LU69338A1 (en)
NL (1) NL174045C (en)
NO (1) NO142260C (en)
PH (1) PH12303A (en)
PL (3) PL97304B1 (en)
SE (1) SE416399B (en)
SU (3) SU715028A3 (en)
YU (1) YU39716B (en)
ZA (1) ZA74472B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT338799B (en) * 1974-03-02 1977-09-12 Boehringer Sohn Ingelheim PROCESS FOR PREPARING NEW SUBSTITUTED 6-ARYL-4H-S-TRIAZOLO- (3,4C) -THIENO- (2,3E) -1,4-DIAZEPINE AND THEIR SALTS
DE2531678C3 (en) * 1975-07-16 1979-06-28 C.H. Boehringer Sohn, 6507 Ingelheim Thieno [2,3e] triazole [3,4c] 5,6-dihydro-1,4-diazepines and processes for their preparation
DE2533924C3 (en) * 1975-07-30 1979-05-03 C.H. Boehringer Sohn, 6507 Ingelheim Process for the preparation of 6-aryl-4H-striazolo [3,4-c] thieno [2,3-e] 1,4-diazepines
DE2708121A1 (en) * 1977-02-25 1978-09-07 Boehringer Sohn Ingelheim TRIAZOLO-THIENO-DIAZEPIN-L-ONE, METHOD FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS
FI63033C (en) * 1977-07-21 1983-04-11 Boehringer Sohn Ingelheim FREQUENCY REQUIREMENT FOR ANXIOLYTIC TRANSQUILLATION OF SEED / ELLER NEUROLEPTIC SUBSTITUTES 1-PIPERAZINYL-4H-S-TRIAZOLO (3,4-C) THIENO (2,3-E) -1,4-DIAZEPERE
DE3502392A1 (en) * 1985-01-25 1986-07-31 Boehringer Ingelheim KG, 6507 Ingelheim NEW THIENO-TRIAZOLO-1,4-DIAZEPINO-2-CARBONIC ACID AMIDES, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITIONS
EP0230942B1 (en) * 1986-01-21 1992-04-29 Boehringer Ingelheim Kg Thieno-1,4-diazepines
JP2582225B2 (en) * 1994-04-15 1997-02-19 ナショナル住宅産業株式会社 Fittings
WO1995032963A1 (en) * 1994-06-01 1995-12-07 Yoshitomi Pharmaceutical Industries, Ltd. Thienylazole compound and thienotriazolodiazepine compound
US5854238A (en) * 1995-09-09 1998-12-29 Hoffmann-La Roche Inc. Use of a thienotriazolodiazephine to increase apolipoprotein A-I levels

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3904641A (en) * 1971-06-18 1975-09-09 Yoshitomi Pharmaceutical Triazolothienodiazepine compounds

Also Published As

Publication number Publication date
JPS49102698A (en) 1974-09-27
FI58129C (en) 1980-12-10
AT343118B (en) 1978-05-10
CH584223A5 (en) 1977-01-31
SE416399B (en) 1980-12-22
SU715028A3 (en) 1980-02-05
YU22874A (en) 1982-06-30
HU173741B (en) 1979-08-28
PL97275B1 (en) 1978-02-28
PL97304B1 (en) 1978-02-28
NO142260B (en) 1980-04-14
GB1456162A (en) 1976-11-17
IE38883L (en) 1974-08-08
NL174045B (en) 1983-11-16
DD112454A5 (en) 1975-04-12
DK137679B (en) 1978-04-17
LU69338A1 (en) 1975-12-09
ZA74472B (en) 1974-11-27
NL174045C (en) 1984-04-16
ATA96474A (en) 1977-09-15
DE2405682B2 (en) 1980-07-17
AU6485574A (en) 1975-07-24
JPS5833234B2 (en) 1983-07-18
DK137679C (en) 1978-09-25
FR2217007B1 (en) 1978-02-03
IL44095A (en) 1979-03-12
NO740405L (en) 1974-08-09
PH12303A (en) 1979-01-16
SU747429A4 (en) 1980-07-23
DE2405682A1 (en) 1974-08-15
BE810705A (en) 1974-08-07
NL7401117A (en) 1974-08-12
FI58129B (en) 1980-08-29
CA1049009A (en) 1979-02-20
IE38883B1 (en) 1978-06-21
SU1060115A3 (en) 1983-12-07
NO142260C (en) 1980-07-23
FR2217007A1 (en) 1974-09-06
AR217034A1 (en) 1980-02-29
HU170423B (en) 1977-06-28
DE2405682C3 (en) 1981-03-12
PL96107B1 (en) 1977-12-31
AR203188A1 (en) 1975-08-22
IL44095A0 (en) 1974-05-16
YU39716B (en) 1985-04-30

Similar Documents

Publication Publication Date Title
GB1456161A (en) Diazepine derivatives
GB1353370A (en) Imidazolpyridine derivatives
ES8801281A1 (en) Benzo-(pyrano and thiopyrano)pyridines.
GB1456627A (en) Pyridobenzodiazepinones
ES8607953A1 (en) Triazine derivatives, processes for preparation thereof and pharmaceutical compositions comprising the same.
AR240828A2 (en) Derivatives of orthocondensed pyrrole useful for the preparation of medicines and their preparation
GB1422266A (en) Diazepine derivatives and processes for their production
GB1460235A (en) Vincaminic acid amides
ATE35259T1 (en) TRIAZINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
GB1351549A (en) 1,3-dhiydro-3-hydroxy-5-phenyl-2h-1,4-benzodiazepin-2-one sub stituted diamino acetate esters and their acid salts
GB1530770A (en) 2,4-imidazolidinedione derivatives and preparation thereo
GB1491858A (en) 1,5-dihydro-2h-1,4-benzodiazepin-2-one derivatives and the production thereof
GB1438260A (en) Sulphoxides and sulphones processes for their preparation and compositions containing them
GB1323591A (en) Benzodiazepine derivatives
GB1332697A (en) Benzodiazepine derivatives
GB1183135A (en) 2,4-Benzodiazepines, process for their manufacture and Compositions containing them
GB1410748A (en) 6-aza-3h-1,4-benzodiazepines
IE35541L (en) Benzodiazepine derivatives.
GB1348449A (en) Benzodiazepine derivatives
GB1497827A (en) Triazolobenzodiazepine derivatives
GB1449426A (en) Phenoxyalkylamine derivatives and preparation therof
GB1325280A (en) 3-substituted-as-triazino-5,6-c-quinolines
GB1260857A (en) IMIDAZO-3H-(4,5-b)-PYRIDINE DERIVATIVES
GB1465993A (en) Fish-treating composition
GB1264737A (en)

Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
704A Declaration that licence is not available as of right for an excepted use (par. 4a/1977)
732 Registration of transactions, instruments or events in the register (sect. 32/1977)
PE20 Patent expired after termination of 20 years

Effective date: 19940206