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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085088생성일: 2026년 10월 27일

N-methyl-N-(trimethylsilyl)trifluoroacetamide → (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/1085088

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
반응물Trimethylsilyl iodideHCID 85247—
반응물CefotaximeHCID 5742673—
용매DichloromethaneHCID 6344—
생성물(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 14252931—

반응 단계

7β-[(Z)-2-(2-Aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (977 mg) was suspended in methylene chloride (16 ml), followed by an addition of N-methyl-N-(trimethylsilyl) trifluoroacetamide (1350 μl). The resulting mixture was stirred at room temperature for 1 hour. After ice-cooling, iodotrimethylsilane (810 μl) was added and the resulting mixture was stirred for 15 minutes. The reaction mixture was concentrated under reduced pressure to obtain the silylated derivative of 7β-[(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05008260
출처 데이터셋uspto-grants-1991_04
ORD IDord-e8783b6d6eb54542a12dccd68b8cb1ca
출처 메모uspto-grants-1991_04