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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1462036생성일: 2026년 10월 27일

Phosphorus pentachloride → benzhydryl (6R)-3-(chloromethyl)-7-[[(2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

https://huagongshe.com/reaction/1462036

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus pentachlorideHCID 24819—
반응물(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acidHCID 5928144—
반응물BistrimethylsilylacetamidHCID 11708267—
반응물Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylateHCID 13239626—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물benzhydryl (6R)-3-(chloromethyl)-7-[[(2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 13239631—

반응 단계

Benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate prepared in Preparation No. 4 (2.29 g, 5.52 mmoles) in CH3CN (57 mL) was treated with bis(trimethylsilyl)acetamide (BSA, 4.09 mL, 16.6 mmoles) at room temperature for 50 minutes to give a clear solution. To the solution was added an acid chloride solution, which was prepared from (Z)-2-methoxyimino-2-(2-tritylaminothiazol-4-yl)acetic acid (IVa) (2.04 g, 4.60 mmoles) and PCl5 (1.15 g, 5.52 mmoles) in methylene chloride (20 mL). The mixture was stirred at room temperature for 30 minutes, poured into cold water (200 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with aqueous NaCl, dried and evaporated. The residual syrup (4 g) was chromatographed on a silica gel (150 g) column by eluting with 10:1 and 3:1 mixtures of toluene and ethyl acetate successively. The fractions containing the desired compound were combined and evaporated to afford 2.61 g (68%) of VIa as an amorphous powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04457929
출처 데이터셋uspto-grants-1984_07
ORD IDord-1f21e603c86f485b89cd61db57985d01
출처 메모uspto-grants-1984_07