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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247921생성일: 2026년 10월 24일

3-Pyridinamine, N,N-dimethyl- → Diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(3-dimethylamino-1-pyridiniomethyl)-3-cephem-4-carboxylate-1-oxide chloride

https://huagongshe.com/ko/reaction/1247921

반응식

참여 물질

역할이름HCID투입량
반응물3-Pyridinamine, N,N-dimethyl-HCID 123378—
반응물Diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate-1-oxideHCID 131714232—
용매TetrahydrofuranHCID 8028—
생성물Diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(3-dimethylamino-1-pyridiniomethyl)-3-cephem-4-carboxylate-1-oxide chlorideHCID 13171423088.8%

반응 단계

A mixture of diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate-1-oxide (syn isomer) (3 g) and 3-dimethylaminopyridine (0.7 g) in tetrahydrofuran (20 ml) was stirred for 2.5 hours at 48° to 50° C. The resulting precipitate was filtered, washed with tetrahydrofuran and dried to give diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(3-dimethylamino-1-pyridiniomethyl)-3-cephem-4-carboxylate-1-oxide chloride (syn isomer) (3.18 g), mp 120° to 130° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04521413
출처 데이터셋uspto-grants-1985_06
ORD IDord-6f97d0a7d6d54560832c5963a9fd8dfa
출처 메모uspto-grants-1985_06