发明名称 PRODUCTION OF VITAMIN D SYNTHETIC INTERMEDIATE
摘要 <p>PURPOSE:To industrially advantageously obtain the subject intermediate, e.g. a synthetic raw material for active vitamin D3s by reducing a specific alkenyl halide compound derived from propargyl alcohol using 0 valent palladium catalyst. CONSTITUTION:p-Methoxybenzylpropagyl ether obtained by protecting hydroxyl group of propargyl alcohol is subjected to lithium acetylide-forming reaction and the reactional product is reacted with epichlorohydrin and further, reacted with t-butyldiphenylsilyl-propargyl ether to afford a compound of formula I (MPM is p-methoxybenzyl; TBDPS is t-butyldiphenylsilyl). Then, hydroxyl group of the compound is protected and either one alkynyl group is reduced and transferred and halogenated with iodine, etc., to give a compound expressed by formula II (X is a halogen; R1 and R2 are each a protecting group) and then, the compound is reduced using 0 valent palladium catalyst to industrially advantageously provide the objective vitamin synthetic intermediate expressed by formula III.</p>
申请公布号 JPH0820590(A) 申请公布日期 1996.01.23
申请号 JP19940155841 申请日期 1994.07.07
申请人 CHUGAI PHARMACEUT CO LTD 发明人 NISHIZAWA MUGIO;HATAYAMA HAN
分类号 B01J23/44;C07F7/18;(IPC1-7):C07F7/18 主分类号 B01J23/44
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