Hydrochloric Acid → 3-{4-[2-(4-Methoxy-2-o-tolylaminobenzoxazol-6-yl)acetylamino]phenyl}butanoic acid
반응식
[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH3:19])[O:11][C:7]=2[CH:6]=[C:5]([CH2:20][C:21]([NH:23][C:24]2[CH:29]=[CH:28][C:27]([C@H:30]([CH3:37])[CH2:31][C:32]([O:34]CC)=[O:33])=[CH:26][CH:25]=2)=[O:22])[CH:4]=1.[OH-].[Li+].Cl>CO>[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH3:19])[O:11][C:7]=2[CH:6]=[C:5]([CH2:20][C:21]([NH:23][C:24]2[CH:25]=[CH:26][C:27]([CH:30]([CH3:37])[CH2:31][C:32]([OH:34])=[O:33])=[CH:28][CH:29]=2)=[O:22])[CH:4]=1참가 물질
실험 절차
A solution of ethyl (R) 3-{4-[2-(4-methoxy-2-o-tolylaminobenzoxazol-6-yl)acetylamino]phenyl}butanoate (0.17 g, Reference Example 8) in methanol was treated with aqueous lithium hydroxide solution (5 mL, 1M) and left to stand for five hours under argon. The mixture was acidified to pH 1 by addition of dilute hydrochloric acid, then partially evaporated, then diluted with more water and then partially evaporated again. The residue was diluted with water to afford a tan solid which was filtered, then dissolved in saturated sodium bicarbonate solution. The solution was washed with ethyl acetate, then acidified to pH1 and then extracted with ethyl acetate several times. The combined ethyl acetate extracts were washed with brine and then evaporated to give the title compound (0.12 g) as a white powder. LC-MS: RT=3.29 minutes (100% by ELSD); MS (ES+), 474 (MH+).
후처리
- waitleft
- custompartially evaporated
- additiondiluted with more water
- custompartially evaporated again
- additionThe residue was diluted with water
- customto afford a tan solid which
- filtrationwas filtered
- dissolutiondissolved in saturated sodium bicarbonate solution
- washThe solution was washed with ethyl acetate
- extractionextracted with ethyl acetate several times
- washThe combined ethyl acetate extracts were washed with brine
- customevaporated
출처 및 근거
- ORD 기록
- ord-b7ffe93854694a15ba030848974e1752
- 출처 데이터셋
- uspto-grants-2003_07
- 특허 번호
- US06593354B2
반응 노트
불러오는 중…