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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984706생성일: 2026년 10월 27일

Triethylamine → 2-(2-tert-Butoxycarbonylaminopyridin-4-ylmethylthio)pyridine-3-carboxylic acid

https://huagongshe.com/reaction/1984706

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물1,1-Dimethylethyl N-[4-(bromomethyl)-2-pyridinyl]carbamateHCID 22097736—
반응물HCID 178524460HCID 178524460—
용매DimethylformamideHCID 6228—
생성물2-(2-tert-Butoxycarbonylaminopyridin-4-ylmethylthio)pyridine-3-carboxylic acidHCID 2315097688%

반응 단계

A solution of triethylamine (0.75 mL, 5.4 mmol) in N,N-dimethylformamide (2.0 mL) was added to a solution of 4-bromomethyl-2-tert-butoxycarbonylaminopyridine (Reference compound No. 8-1, 500 mg, 1.7 mmol) and 2-mercaptonicotinic acid (270 mg, 1.7 mmol) in N,N-dimethylformamide (3.0 mL) under ice-cooling, and the mixture was stirred for 12 hours at room temperature. Ethyl acetate (20 mL) was added to the reaction mixture, and the whole was extracted with 0.1N aqueous sodium hydroxide solution (50 mL). 1N Hydrochloric acid was added to the aqueous layer to adjust to pH 5, and the precipitated crystal was filtered off. The crystal was dried under reduced pressure at 60° C. to give 560 mg of the title reference compound as a colorless crystal. (Yield 88%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544703B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-27456374c0c8432d940c7742997ad096
출처 메모uspto-grants-2009_06