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

HRID 1984706

반응식

HRID 1984706 반응식
C(N(CC)CC)C.Br[CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH:11]=1.[SH:24][C:25]1[N:33]=[CH:32][CH:31]=[CH:30][C:26]=1[C:27]([OH:29])=[O:28].C(OCC)(=O)C>CN(C)C=O>[C:20]([O:19][C:17]([NH:16][C:12]1[CH:11]=[C:10]([CH2:9][S:24][C:25]2[C:26]([C:27]([OH:29])=[O:28])=[CH:30][CH:31]=[CH:32][N:33]=2)[CH:15]=[CH:14][N:13]=1)=[O:18])([CH3:23])([CH3:22])[CH3:21]

참가 물질

6

실험 절차

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%)

후처리

  1. extractionthe whole was extracted with 0.1N aqueous sodium hydroxide solution (50 mL)
  2. addition1N Hydrochloric acid was added to the aqueous layer
  3. filtrationthe precipitated crystal was filtered off
  4. customThe crystal was dried under reduced pressure at 60° C.
  5. customto give 560 mg of the title reference compound as a colorless crystal

출처 및 근거

ORD 기록
ord-27456374c0c8432d940c7742997ad096
출처 데이터셋
uspto-grants-2009_06
특허 번호
US07544703B2

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