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公开(公告)号:ES2136669T3
公开(公告)日:1999-12-01
申请号:ES94100048
申请日:1994-01-04
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
Abstract: The invention relates to a method for the preparation of a compound of the general formula (I) in which X represents an optionally protected formyl group and R denotes a group which is itself inert to the reaction conditions of the synthesis, for example -CN, characterised in that a compound of the general formula (II) where X is as defined above, is reacted with a substituted phenyl halogen compound of the formula (III) where Hal denotes e.g. bromine. The compounds are useful intermediates for pharmaceutical synthesis.
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公开(公告)号:CZ1494A3
公开(公告)日:1994-08-17
申请号:CZ1494
申请日:1994-01-04
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
Abstract: The invention relates to a method for the preparation of a compound of the general formula (I) in which X represents an optionally protected formyl group and R denotes a group which is itself inert to the reaction conditions of the synthesis, for example -CN, characterised in that a compound of the general formula (II) where X is as defined above, is reacted with a substituted phenyl halogen compound of the formula (III) where Hal denotes e.g. bromine. The compounds are useful intermediates for pharmaceutical synthesis.
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公开(公告)号:AT183732T
公开(公告)日:1999-09-15
申请号:AT94100048
申请日:1994-01-04
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
Abstract: The invention relates to a method for the preparation of a compound of the general formula (I) in which X represents an optionally protected formyl group and R denotes a group which is itself inert to the reaction conditions of the synthesis, for example -CN, characterised in that a compound of the general formula (II) where X is as defined above, is reacted with a substituted phenyl halogen compound of the formula (III) where Hal denotes e.g. bromine. The compounds are useful intermediates for pharmaceutical synthesis.
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公开(公告)号:DK0606065T3
公开(公告)日:2000-03-13
申请号:DK94100048
申请日:1994-01-04
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
Abstract: The invention relates to a method for the preparation of a compound of the general formula (I) in which X represents an optionally protected formyl group and R denotes a group which is itself inert to the reaction conditions of the synthesis, for example -CN, characterised in that a compound of the general formula (II) where X is as defined above, is reacted with a substituted phenyl halogen compound of the formula (III) where Hal denotes e.g. bromine. The compounds are useful intermediates for pharmaceutical synthesis.
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公开(公告)号:GR3031852T3
公开(公告)日:2000-02-29
申请号:GR990402946
申请日:1999-11-17
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
Abstract: The invention relates to a method for the preparation of a compound of the general formula (I) in which X represents an optionally protected formyl group and R denotes a group which is itself inert to the reaction conditions of the synthesis, for example -CN, characterised in that a compound of the general formula (II) where X is as defined above, is reacted with a substituted phenyl halogen compound of the formula (III) where Hal denotes e.g. bromine. The compounds are useful intermediates for pharmaceutical synthesis.
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公开(公告)号:CZ9400014A3
公开(公告)日:1994-08-17
申请号:CZ1494
申请日:1994-01-04
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , BHATNAGAR NEERJA DR , BUENDIA JEAN DR , GRIFFOUL CHRISTINE DR
IPC: B01J23/44 , A61K31/235 , A61K31/41 , C07B37/04 , C07B61/00 , C07C41/48 , C07C45/61 , C07C45/71 , C07C47/546 , C07C67/30 , C07C67/343 , C07C69/76 , C07C69/767 , C07C253/30 , C07C255/37 , C07C255/40 , C07C255/56 , C07C303/40 , C07C311/09 , C07C311/48 , C07C311/51 , C07C311/52 , C07C311/53 , C07C311/54 , C07C311/57 , C07C311/58 , C07D257/04
CPC classification number: C07D257/04 , C07B37/04 , C07C67/343 , C07C253/30 , C07C303/40 , C07C311/09 , C07C311/51 , C07C311/58 , C07C69/76
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