Acetic Acid → (2S)-2-acetamido-5-[[(2R)-1-(carboxymethylamino)-1-oxo-3-sulfanylpropan-2-yl]amino]-5-oxopentanoic acid

HRID 1867912노트

반응식

HRID 1867912 반응식
[NH2:1][C@@H:2]([CH2:6][CH2:7][C:8]([NH:10][C@H:11]([C:14]([NH:16][CH2:17][C:18]([OH:20])=[O:19])=[O:15])[CH2:12][SH:13])=[O:9])[C:3]([OH:5])=[O:4].[C:21](OC(=O)C)(=[O:23])[CH3:22].C(O)(=O)C.C(OCC)C>O>[C:21]([NH:1][C@@H:2]([CH2:6][CH2:7][C:8]([NH:10][C@H:11]([C:14]([NH:16][CH2:17][C:18]([OH:20])=[O:19])=[O:15])[CH2:12][SH:13])=[O:9])[C:3]([OH:5])=[O:4])(=[O:23])[CH3:22]

참가 물질

6

실험 절차

A solution of glutathione (1 g, 3.25 mmole) in 10 ml of water was added over 1 hr to a mixture of acetic anhydride (10 ml) and acetic acid (10 ml) at room temperature. After the addition was complete, the reaction mixture was chilled on ice. Additional acetic anhydride (5 ml) was added and the reaction mix was stirred while it gradually warmed to room temperature overnight. The reaction mixture was treated with 300 ml of ethyl ether and cooled overnight to obtain crystallized product. A white solid was obtained by filtering the reaction mix, and washing with more ether. More crystallized product was generated in the filtrate. The filtration and washing were repeated a second time and the white solids were combined and air-dried (585 mg, yield 51.5%).

후처리

  1. additionAfter the addition
  2. temperaturethe reaction mixture was chilled on ice
  3. additionthe reaction mix
  4. temperaturecooled overnight
  5. customto obtain
  6. customcrystallized product
  7. customA white solid was obtained
  8. filtrationby filtering the reaction
  9. additionmix
  10. washwashing with more ether
  11. customMore crystallized product
  12. filtrationThe filtration
  13. washwashing
  14. customair-dried (585 mg, yield 51.5%)

출처 및 근거

ORD 기록
ord-5fb09e9acc764c87a781c2d14a8fa214
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07632928B2

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