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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 1,1-Dimethylethyl N-[4-(bromomethyl)-2-pyridinyl]carbamate | HCID 22097736 | — |
| 반응물 | HCID 178524460 | HCID 178524460 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(2-tert-Butoxycarbonylaminopyridin-4-ylmethylthio)pyridine-3-carboxylic acid | HCID 23150976 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07544703B2 |
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| 출처 데이터셋 | uspto-grants-2009_06 |
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| ORD ID | ord-27456374c0c8432d940c7742997ad096 |
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| 출처 메모 | uspto-grants-2009_06 |
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