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公开(公告)号:DE4341400A1
公开(公告)日:1995-06-08
申请号:DE4341400
申请日:1993-12-04
Applicant: BASF AG
Inventor: STEINER GERD DR , MUNSCHAUER RAINER DR , UNGER LILIANE DR , TESCHENDORF HANS-JUERGEN DR ME , HOEGER THOMAS DR
IPC: C07D209/72 , A61K31/40 , C07D417/06 , C07D471/18 , C07D487/18 , C07D491/18
Abstract: 4,7-Bridged tetra- or hexa hydro-isoindoline derivs. of formula (I) and their acid-addn. salts are new. B = CH2, C2H4, NH, NMe or NCOMe; R1 = H or phenyl, opt. mono- or disubstd. by halo, 1-4C alkyl, CF3, OH, 1-4C alkoxy, NH2, NHMe, NMe2, CN or NO2; n = 0-4; A = H, CR2R4, N(R5)COR4, N(R5)SO2R4, OSO2R4, CH = CHR4, or CH=C(R4)2; R2 = H, OH, or phenyl opt. substd. by F, Cl or Br; R3 = H; or R2 + R3 = O; R4 = phenyl, or thienyl opt. mono- or disubstd. by F, Cl, Br, OH, NO2, NH2, 1-4C alkanoylamino, 1-4C alkylamino, 1-4C alkyl or OMe; R5 = H or Me.
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22.
公开(公告)号:DE4338397A1
公开(公告)日:1995-05-11
申请号:DE4338397
申请日:1993-11-10
Applicant: BASF AG
Inventor: STEINER GERD DR , MUNSCHAUER RAINER DR , UNGER LILIANE DR , TESCHENDORF HANS-JUERGEN DR ME , HOEGER THOMAS DR
IPC: C07D403/06 , C07D491/18 , A61K31/505 , A61K31/53 , A61K31/54 , C07D471/04 , C07D513/04 , C07D519/00
Abstract: Compounds of the formula I wherein B, R , R , n, A, X, Y, Z and the 5,6 bond have the meaning indicated in the description, and their preparation are described. The novel compounds are suitable for the control of diseases.
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公开(公告)号:DE4119756A1
公开(公告)日:1992-12-17
申请号:DE4119756
申请日:1991-06-15
Applicant: BASF AG
IPC: A61K31/435 , A61K31/425 , A61K31/426 , A61K31/427 , A61K31/4439 , A61K31/454 , A61K31/495 , A61K31/496 , A61P9/12 , A61P25/16 , A61P25/18 , C07D277/20 , C07D277/40 , C07D277/54 , C07D417/12 , C07D417/14
Abstract: Described are aminoalkyl-substituted 5-mercaptothiazoles of formula (I), in which R , n and A are as defined in the description, as well as their preparation. The compounds are suitable for use in the treatment of illnesses.
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公开(公告)号:DE3834861A1
公开(公告)日:1990-04-19
申请号:DE3834861
申请日:1988-10-13
Applicant: BASF AG
IPC: A61K31/00 , A61K31/37 , A61P25/00 , A61P25/02 , A61P25/04 , A61P25/16 , A61P25/24 , A61P25/26 , A61P25/28 , C07D311/16
Abstract: Arylalkoxycoumarins of the general formula I I where R1 and R2 independently of one another are each hydrogen, lower alkyl, phenyl or halogen, or the two radicals together form an alkylene bridge of 3 to 5 carbon atoms, R3 is lower alkyl or halogen, n is an integer of from 0 to 3, m is an integer of from 0 to 4, R4 is hydrogen or lower alkyl and Ar is a phenyl ring which is monosubstituted to trisubstituted by halogen, C1-C6-alkyl or C1-C6-alkoxy or monosubstituted by nitro, cyano or trifluoromethyl or is a naphthyl ring, with the proviso that m is not 0 when Ar is unsubstituted phenyl, processes for their preparation, and drugs prepared therefrom.
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公开(公告)号:DE3436550A1
公开(公告)日:1985-04-25
申请号:DE3436550
申请日:1984-10-05
Applicant: BASF AG
Inventor: SCHLECKER RAINER DR , KROPP RUDOLF , REICHENEDER FRANZ DR , GRIES JOSEF DR MED , HOFMANN HANS PETER DR , TESCHENDORF HANS-JUERGEN DR ME , TRAUT MARTIN DR
IPC: C07D237/20 , A61K31/50
Abstract: 1-Phenyl-4(1H)-pyridazinone imines substituted on the imine nitrogen atom, of the formula (I) and their acid addition salts with a physiologically tolerated acid, process for their preparation, pharmaceutical formulations containing these compounds, and their use as drugs, especially as antidepressants, antiparkinson drugs and antihypotensives.
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公开(公告)号:DE3243518A1
公开(公告)日:1984-05-30
申请号:DE3243518
申请日:1982-11-25
Applicant: BASF AG
Inventor: SEITZ WERNER DR , MICHEL ALFRED , TESCHENDORF HANS-JUERGEN DR ME , KREISKOTT HORST PROF DR , HOFMANN HANS PETER DR , TRAUT MARTIN DR
IPC: C07C225/18 , A61K31/135 , A61K31/205 , A61K31/395 , A61P25/24 , A61P25/26 , C07D207/08 , C07D211/32 , C07D295/10 , C07D295/116 , C07D295/12 , C07D295/145 , C07C97/10
Abstract: 1-Oxo-2-phenyl-2-(2-alkylaminoethyl)-1,2,3,4-tetrahydronaphthalenes of the formula I I where R1 and R2 are identical or different and are each hydrogen, halogen, trifluoromethyl, C1-C4-alkyl or C1-C4-alkoxy, R3 is C1-C6-alkyl and R4 is hydrogen, C1-C6-alkyl or benzyl, or R3 and R4 together may furthermore be a C2-C5-alkylene chain, and their salts with physiologically tolerated acids, and their preparation, are described. The novel compounds are useful active compounds for treating disorders.
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公开(公告)号:DE3242477A1
公开(公告)日:1984-05-24
申请号:DE3242477
申请日:1982-11-18
Applicant: BASF AG
Inventor: FRANKE ALBRECHT DR , STEINER GERD DR , HOFMANN HANS PETER DR , MUELLER CLAUS D DR MED , TESCHENDORF HANS-JUERGEN DR ME
IPC: A61K31/40 , A61K31/403 , A61K31/4035 , A61K31/425 , A61K31/428 , A61P25/20 , A61P25/24 , A61P25/26 , C07D209/46 , C07D209/48 , C07D275/04 , C07D275/06 , C07D495/04 , C07D513/04
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公开(公告)号:DE3108427A1
公开(公告)日:1982-09-23
申请号:DE3108427
申请日:1981-03-06
Applicant: BASF AG
Inventor: STEINER GERD DIPL CHEM DR , HOFMANN HANS PETER DR , KREISKOTT HORST DR , TESCHENDORF HANS-JUERGEN DR ME
IPC: C07D263/20 , C07D495/14 , C07D413/14 , A61K31/42 , A61K31/495 , A61K31/55 , C07D409/14 , C07D413/06 , C07D495/06
Abstract: The invention relates to tricyclic 3-[2-(1-piperazinyl)ethyl]-2-oxazolidinone derivatives, process for their preparation and therapeutic compositions which contain them and can be used as sedatives, hypnotics, tranquillisers or neuroleptics.
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公开(公告)号:DE4427647A1
公开(公告)日:1996-02-08
申请号:DE4427647
申请日:1994-08-04
Applicant: BASF AG
Inventor: STEINER GERD DR , MUNSCHAUER RAINER DR , HOEGER THOMAS DR , UNGER LILIANE DR , TESCHENDORF HANS-JUERGEN DR ME
IPC: C07D409/12 , A61K31/40 , A61K31/403 , A61P25/18 , A61P43/00 , C07D209/44 , C07D209/52 , C07D209/90 , C07D209/92 , C07D403/06 , C07D209/80 , C07D209/34 , A61K31/645
Abstract: New compounds having the formula (I), in which A, R and n have the meanings given in the description, are useful for fighting diseases.
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公开(公告)号:DE4425146A1
公开(公告)日:1996-01-18
申请号:DE4425146
申请日:1994-07-15
Applicant: BASF AG
Inventor: HELLENDAHL BEATE DR , LANSKY ANNEGRET DR , RENDENBACH-MUELLER BEATRICE DR , BACH ALFRED DR , UNGER LILIANE DR , TESCHENDORF HANS-JUERGEN DR ME , WICKE CARSTEN DR
IPC: C07D233/84 , A61K31/33 , A61K31/415 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4418 , A61K31/4425 , A61K31/445 , A61K31/495 , A61K31/496 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , C07D213/56 , C07D213/64 , C07D213/65 , C07D213/70 , C07D213/73 , C07D213/79 , C07D213/81 , C07D233/90 , C07D307/79 , C07D333/24 , C07D333/28 , C07D333/38 , C07D471/18 , A61K31/52
Abstract: The present invention relates to the use of heterocyclic compounds of formula (I) Het - A - B - Ar in which Het A, B and Ar have the meanings given in the description. The compounds of the invention have a high affinity for the dopamine-D3-receptor and are therefore usable for the treatment of diseases responding to dopamine-D3-ligands.
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