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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27138생성일: 2026년 10월 24일

Dimethylformamide → HCID 178451131, 화합물

https://huagongshe.com/ko/reaction/27138

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물alpha-t-ButoxycarbonylthienylacetamideHCID 21315147—
반응물HCID 178508097HCID 178508097—
촉매FormamideHCID 713—
용매Diethyl EtherHCID 3283—
생성물HCID 178451131HCID 178451131—

반응 단계

7-Amino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (1.0 g., 2.68 mmol.) was suspended in 10 ml. of dry dimethylformamide and 1.12 ml of triethylamine was added followed by 85 drops of formamide. A solution of 0.91 g. (2.68 mmol.) of the activated ester of α-t-butoxycarbonylthienylacetamide, prepared as described above, in 2 ml. of dimethylformamide was added and the reaction mixture was stirred at 25° for three hours. An additional 0.45 g. of activated ester was then added and the mixture stirred another five hours. Ether (ca. 300 ml.) was added and the solution was decanted. The remaining oily material was washed with ether, dissolved in water and the aqueous solution was extracted with ethyl acetate. The pH of the ethyl acetate solution was adjusted to 1.5 by addition of dilute hydrochloric acid. Extraction with ethyl acetate and evaporation of the solvent gave 7-(α-t-butoxycarbonylthienylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220644
출처 데이터셋uspto-grants-1980_09
ORD IDord-0814228fd3c04f48a650f123d503d391
출처 메모uspto-grants-1980_09