Hydrochloric Acid → S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteine

HRID 486877

반응식

HRID 486877 반응식
[CH2:1]([S:8][CH2:9][C@@H:10]([C:12]([OH:14])=[O:13])[NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:15]([S:22][CH2:23][C:24]([CH3:29])([CH3:28])[C:25](Cl)=[O:26])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.Cl>[OH-].[Na+].CCOCC>[CH2:1]([S:8][CH2:9][C@@H:10]([C:12]([OH:14])=[O:13])[NH:11][C:25](=[O:26])[C:24]([CH3:28])([CH3:29])[CH2:23][S:22][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

6

실험 절차

To a stirred solution of S-benzyl-L-cysteine(11.5 g) in 2N sodium hydroxide solution(68 ml), 3-benzylthio-2,2-dimethylpropionyl chloride (14.6 g) dissolved in ether(10 ml) was added dropwise under ice-cooling. After the addition, the reaction mixture was stirred for 20 minutes under ice-cooling and 2 hours at room temperature. The reaction mixture was acidified with 6N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The oily residue was purified by a silica gel column chromatography to give 19.4 g(85.1%) of the titled compound.

후처리

  1. additionwas added dropwise under ice-
  2. temperaturecooling
  3. additionAfter the addition
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with saturated sodium chloride solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe oily residue was purified by a silica gel column chromatography

출처 및 근거

ORD 기록
ord-794df2e6979d43a08be0468fd21596f8
출처 데이터셋
uspto-grants-1994_03
특허 번호
US05292926

연결된 노트

불러오는 중…