Hydrochloric Acid → HCID 59519252, 화합물
반응식
Cl.[CH2:2]([NH:4][C:5]([C:7]1[S:33][C:10]2[N:11]=[C:12]([NH2:32])[N:13]=[C:14]([C:15]3[CH:20]=[C:19]([O:21][CH2:22][CH:23](OCC)OCC)[C:18]([Cl:30])=[CH:17][C:16]=3[Cl:31])[C:9]=2[CH:8]=1)=[O:6])[CH3:3].[NH:34]1[CH2:39][CH2:38][O:37][CH2:36][CH2:35]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C1COCC1.ClCCl>[CH2:2]([NH:4][C:5]([C:7]1[S:33][C:10]2[N:11]=[C:12]([NH2:32])[N:13]=[C:14]([C:15]3[CH:20]=[C:19]([O:21][CH2:22][CH2:23][N:34]4[CH2:39][CH2:38][O:37][CH2:36][CH2:35]4)[C:18]([Cl:30])=[CH:17][C:16]=3[Cl:31])[C:9]=2[CH:8]=1)=[O:6])[CH3:3]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
Hydrochloric acid was added to a solution of 2-Amino-4-(2,4-dichloro-5-(2,2-diethoxyethoxy)-phenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl amide in THF and the solution stirred for ˜18 hrs. Morpholine was added and the solution stirred, sodium triacetoxyborohydride was added and the resulting suspension stirred for ˜18 hrs. Dichloromethane was added and the mixture washed with aqueous ammonia (0.880), water and saturated aqueous sodium chloride solution. The solution was dried over anhydrous sodium sulphate and concentrated to a pale yellow solid. The crude product was purified by chromatography on silica eluting with mixtures of ethyl acetate and hexane.
후처리
- stirringthe solution stirred
- stirringthe resulting suspension stirred for ˜18 hrs
- washthe mixture washed with aqueous ammonia (0.880), water and saturated aqueous sodium chloride solution
- dry with materialThe solution was dried over anhydrous sodium sulphate
- concentrationconcentrated to a pale yellow solid
- customThe crude product was purified by chromatography on silica eluting with mixtures of ethyl acetate and hexane
출처 및 근거
- ORD 기록
- ord-10c0e1f734cc4841a8db615562fc7c4a
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642594B2
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