发明名称 PROCESS FOR PREPARING CEPHEM INTERMEDIATES
摘要 <p>Cephem intermediates(I; A,B = H, amino substituent; R = H, thiol substituent; X = hydroxy, carboxy protecting group; Z = sulfonyl group) were prepd. by treating compd.(II) with substituted amine. Thus, benzylchloroformate 100 mg was added in the tetrahydrofurane 3 ml soln. of methylα-[4-mercapto-3-phthalimido-2-oxoazetidine-1-yl -α-(1-hydroxyethylidene) acetate 100 mg and then cooled to -65oC. Triethylamine 60 mg was added in the soln., heated to the room temp. and then evapd. The residue was purified with silica gel chromatography to give methylα-[4-benzyloxycarbonylthio-3-phthalimido-2-oxoazetidine-1-yl -α-(1-benzyloxycarbonylethylidene)acetate 160 mg.</p>
申请公布号 KR810001428(B1) 申请公布日期 1981.10.21
申请号 KR19790004492 申请日期 1979.12.18
申请人 SHIONOKI PHARMA CO LTD 发明人 KOMENO TAICHIRO;YOSHIOKA MITSURU;TSUJI TERUJI;HAMAJIMA YOSHIO;TANIDA HIROSHI;NARISADA MASAYUKI
分类号 C07D513/04;(IPC1-7):07D513/04 主分类号 C07D513/04
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