Hydrochloric Acid → 4-(4-Fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenylamino)thieno[2,3-d]pyrimidine-6-carboxylic acid
반응식
O.[OH-].[Li+].[F:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:13]3[CH:20]=[C:19]([C:21]([O:23]C)=[O:22])[S:18][C:14]=3[N:15]=[CH:16][N:17]=2)=[C:7]([O:25][CH:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)[CH:6]=1.Cl>C1COCC1.O>[F:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:13]3[CH:20]=[C:19]([C:21]([OH:23])=[O:22])[S:18][C:14]=3[N:15]=[CH:16][N:17]=2)=[C:7]([O:25][CH:26]2[CH2:27][CH2:28][O:29][CH2:30][CH2:31]2)[CH:6]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
Lithium hydroxide monohydrate (0.062 g, 1.49 mmol) was added into a suspension of methyl 4-(4-fluoro-2-(tetrahydro-2H-pyran-4-yloxy)phenylamino)thieno[2,3-d]pyrimidine-6-carboxylate (0.100 g, 0.25 mmol) in THF/water (1:1; 1.0 mL) and the reaction stirred at ambient temperature for 16 hours. The mixture was cooled in an ice-bath and 1 N hydrochloric acid added drop wise until the solution reached pH 5. The precipitate was collected, washed with water and dried over P2O5 to yield off-white solid (0.060 g, 62%).
후처리
- temperatureThe mixture was cooled in an ice-bath
- customThe precipitate was collected
- washwashed with water
- dry with materialdried over P2O5
출처 및 근거
- ORD 기록
- ord-fb30df056e694a98a72e003b695c6e69
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08486953B2
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