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公开(公告)号:AT49757T
公开(公告)日:1990-02-15
申请号:AT86111840
申请日:1986-08-27
Applicant: HOECHST AG
Inventor: REUSCHLING DIETER DR , LINKIES ADOLF DR , REIMANN WALTER DR , SCHWEIKERT OTTO ERNST DR , MACK KARL ERNST DR
IPC: A23L27/20 , A23L27/30 , C07D291/06
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公开(公告)号:AT76638T
公开(公告)日:1992-06-15
申请号:AT87105537
申请日:1987-04-14
Applicant: HOECHST AG
Inventor: LOHAUS GERHARD DR , DITTMAR WALTER DR , HAENEL HEINZ DR , RAETHER WOLFGANG DR , REUSCHLING DIETER DR , GROEBEL BENGT-THOMAS DR
IPC: A61K31/44 , C07D213/89 , C07D309/38
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公开(公告)号:AT49201T
公开(公告)日:1990-01-15
申请号:AT86111841
申请日:1986-08-27
Applicant: HOECHST AG
Inventor: REUSCHLING DIETER DR , LINKIES ADOLF DR , REIMANN WALTER DR , SCHWEIKERT OTTO ERNST DR , MACK KARL ERNST DR , EBERTZ WOLFGANG DR
IPC: A23L27/20 , A23L27/30 , C07D291/06
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4.
公开(公告)号:CS262439B2
公开(公告)日:1989-03-14
申请号:CS632386
申请日:1986-09-01
Applicant: HOECHST AG
Inventor: REUSCHLING DIETER DR , LINKIES ADOLF DR , REIMANN WALTER DR , SCHWEIKERT OTTO E DR , MACK KARL E DR , EBERTZ WOLFGANG DR
IPC: A23L27/20 , A23L27/30 , C07D291/06
Abstract: The non-toxic salts of 6-methyl-3,4-dihydro-1,2,3-oxothiazin-4-one 2,2-dioxide are prepared by cyclizing acetoacetamide-N-sulfonic acid or its salts with an at least approximately equimolar amount of SO3 in the presence of a water-immiscible, inert organic solvent and, if appropriate, also an inert inorganic solvent, hydrolyzing the 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide obtained in the form of the SO3-adduct after the cyclization reaction, in the event that the amount of SO3 employed is more than equimolar, purifying the organic phase (which has separated out) by extraction with a small volume of water or dilute aqueous sulfuric acid, preferably only with water, and isolating, by neutralization with bases, the non-toxic salts of the 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide from the organic phase thus purified. The said salts are obtained in this process in an extremely pure form; they are valuable synthetic sweetening agents. The potassium salt is known as acesulfam (K).
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公开(公告)号:DE4104931A1
公开(公告)日:1992-08-20
申请号:DE4104931
申请日:1991-02-18
Applicant: HOECHST AG
Inventor: ERKER GERHARD PROF DR , NOLTE REINER DR , AULBACH MICHAEL DR , WEISS ASTRID , REUSCHLING DIETER DR , ROHRMANN JUERGEN DR
IPC: C07C1/207 , C07C1/24 , C07C2/86 , C07C13/465 , C07C17/26 , C07C22/08 , C07C25/22 , C07C43/21 , C07C43/267 , C07C43/29 , C07D213/06 , C07D213/16 , C07D233/08 , C07D307/36 , C07D307/42 , C07D333/08 , C07D335/02 , C07F7/08
Abstract: The compounds of the formula I or Ia (I) (Ia) in which R1 is alkyl, aryl, alkoxy, alkenyl, arylalkyl, alkylaryl, aryloxy, fluoroalkyl, halogenoaryl, alkynyl, trialkylsilyl or a heteroaromatic radical, R2, R3 and R4, in addition to hydrogen, have the meanings given under R1 and R5 is hydrogen, alkyl, fluoroalkyl or alkenyl, can be obtained in a one-stage process by reaction of a compound II with (substituted) cyclopentadiene in the presence of a base. The compounds I and Ia are suitable as ligands for metallocene complexes which are used as catalysts in olefin polymerization.
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公开(公告)号:DE3779352D1
公开(公告)日:1992-07-02
申请号:DE3779352
申请日:1987-04-14
Applicant: HOECHST AG
Inventor: LOHAUS GERHARD DR , DITTMAR WALTER DR , HAENEL HEINZ DR , RAETHER WOLFGANG DR , REUSCHLING DIETER DR , GROEBEL BENGT-THOMAS DR
IPC: A61K31/44 , C07D213/89 , C07D309/38
Abstract: (A) 1-Hydroxy-2-pyridones of formula (I) are new: R1-R3 = H or 1-4C alkyl; X = O or S; Y = H or up to 2 halogen atoms, i.e. Cl and/or Br; Z = a direct bond, O, S, C(R)2, or 2-10C alkylene or alkenylenemm (opt. substd. by 1-4C alkyl) in which one or more C atoms may be replaced by O and/or S, provided that these are sepd. by at least 2C atoms. R = H or 1-4C alkyl; Ar = mono- or bicyclic aryl opt. substd. by up to 3 of F, Cl, Br, OMe, 1-4C alkyl, CF3 and OCF3. (B) Intermediates of formula (IV) are also new. Specifically R1 = R3 = A; R2 = Me; X = O; Z = a bond, O or an O-contg. gp.; Ar = opt. substd. phenyl , biphenyl, phenylalkylphenyl or phenoxyphenyl.
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公开(公告)号:CS8606323A2
公开(公告)日:1988-07-15
申请号:CS632386
申请日:1986-09-01
Applicant: HOECHST AG
Inventor: REUSCHLING DIETER DR , LINKIES ADOLF DR , REIMANN WALTER DR , SCHWEIKERT OTTO E DR , MACK KARL E DR , EBERTZ WOLFGANG DR
IPC: A23L27/20 , A23L27/30 , C07D291/06 , A23L1/236
CPC classification number: C07D291/06
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公开(公告)号:DE3560081D1
公开(公告)日:1987-04-09
申请号:DE3560081
申请日:1985-03-09
Applicant: HOECHST AG
Inventor: LINKIES ADOLF DR , REUSCHLING DIETER DR
IPC: A23L27/30 , B01J27/00 , B01J27/232 , C07B61/00 , C07C67/00 , C07C301/00 , C07C303/36 , C07C307/00 , C07C307/02 , C07C311/00 , C07D291/06 , C07C143/86
Abstract: Crystalline salts of acetoacetamide-N-sulfofluoride are prepared by reacting amidosulfofluoride H2NSO2F with diketene in the presence of inorganic bases, preferably alkali metal carbonates and/or hydrogencarbonates, in particular potassium carbonate, in an inert organic solvent. The salts can be further processed with further base, for example with methanolic KOH, into salts of 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide; the potassium salt, in particular, is important for use as a sweetener ("Acesulfame").
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公开(公告)号:DE3410440A1
公开(公告)日:1985-09-26
申请号:DE3410440
申请日:1984-03-22
Applicant: HOECHST AG
Inventor: CLAUSS KARL DR , LINKIES ADOLF DR , REUSCHLING DIETER DR
IPC: A23L27/30 , C07D291/06 , A23L1/236
Abstract: 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide is prepared by reaction of acetoacetamide with at least approximately twice the molar amount of SO3 per mole of acetoacetamide, if appropriate in an inert inorganic or organic solvent. Relevant salts can be obtained, using bases, from the product which results in the form of the acid. The non-toxic salts, in particular the potassium salt, are valuable synthetic sweeteners.
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公开(公告)号:DE2524955A1
公开(公告)日:1977-03-17
申请号:DE2524955
申请日:1975-06-05
Applicant: HOECHST AG
Inventor: BARTMANN WILHELM DR , BECK GERHARD DR , REUSCHLING DIETER DR , SEEGER KARL DR , TEUFEL HERMANN DR
IPC: C07D333/16 , A61K31/557 , A61K31/5575 , A61P1/04 , A61P7/02 , A61P7/10 , A61P9/12 , A61P43/00 , C07C67/00 , C07C401/00 , C07C405/00 , C07D307/935 , C07D333/00 , C07D333/32 , C07D333/64 , C07D333/78 , C07D409/12 , C07D409/14 , C07F9/54 , C07C177/00 , C07D307/93 , A61K31/38
Abstract: The present invention relates to thienyl-prostaglandin derivatives and to a process for their manufacture. The compounds according to the invention have valuable pharmaceutical properties.
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