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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26039생성일: 2026년 10월 24일

N,N-Diethylaniline → Benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate

https://huagongshe.com/ko/reaction/26039

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylanilineHCID 7061—
반응물Cyanomethylthioacetyl chlorideHCID 19989189—
반응물benzhydryl 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylateHCID 131711470—
용매TetrahydrofuranHCID 8028—
생성물Benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylateHCID 131711469—

반응 단계

To 244 mg of benzhydryl 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate in 20 ml of anhydrous tetrahydrofuran were added dropwise at -7° C. with stirring 115 mg of N,N-diethylaniline and, subsequently, 115 mg of cyanomethylthioacetyl chloride in 5 ml of anhydrous tetrahydrofuran. After completion of the reaction, the reaction mixture was then treated in the same manner as in Example 1--(a) to give a crude product. The crude product was purified by developing it with ethyl acetate by the use of silica gel thin layer chromatography (20×20×0.2 cm) to yield 50 mg of benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147863
출처 데이터셋uspto-grants-1979_04
ORD IDord-9ccf351a7ed6494b8dcd9d01fb533e95
출처 메모uspto-grants-1979_04