Hydrochloric Acid → 2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]-6-methylbenzoic acid
반응식
C(=O)([O-])[O-].[Na+].[Na+].[CH3:7][C:8]1[C:13]([C:14]([OH:16])=[O:15])=[C:12]([NH:17][C:18](=[O:24])[C@H:19]([CH:21]([CH3:23])[CH3:22])[NH2:20])[CH:11]=[CH:10][CH:9]=1.[CH:25]1[C:37]2[CH:36]([CH2:38][O:39][C:40](Cl)=[O:41])[C:35]3[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=3)[C:29]=2[CH:28]=[CH:27][CH:26]=1.Cl>O1CCOCC1.O>[CH:25]1[C:37]2[CH:36]([CH2:38][O:39][C:40]([NH:20][C@H:19]([C:18]([NH:17][C:12]3[CH:11]=[CH:10][CH:9]=[C:8]([CH3:7])[C:13]=3[C:14]([OH:16])=[O:15])=[O:24])[CH:21]([CH3:22])[CH3:23])=[O:41])[C:35]3[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=3)[C:29]=2[CH:28]=[CH:27][CH:26]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
284 mg of sodium carbonate and 336 mg of 6-methyl-2-(L-valylamino)benzoic acid were dissolved in a mixture consisting of 17 ml of 1,4-dioxane and 12 ml of water, followed by adding dropwise a solution of 345 mg of 9-fluorenylmethoxycarbonyl chloride in 7 ml of 1,4-dioxane under ice-cooling. After stirring for 3.5 hours at room temperature, the reaction mixture was poured into water, acidified with concentrated hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with a saturated saline, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by a silica gel column chromatography (eluting solution: hexane-ethyl acetate-acetic acid) to give 460 mg of 2-{[N-(9-fluorenylmethoxy-carbonyl)-L-valyl]amino}-6-methylbenzoic acid.
후처리
- temperaturecooling
- extractionextracted with ethyl acetate
- washThe organic layer was washed with a saturated saline
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by a silica gel column chromatography (eluting solution: hexane-ethyl acetate-acetic acid)
출처 및 근거
- ORD 기록
- ord-98f7ba6898274906aafe4bd2ca3c9145
- 출처 데이터셋
- uspto-grants-1994_07
- 특허 번호
- US05332734
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