Hydrochloric Acid → N-(7-(2-Fluoro-4-iodophenylamino)-8-fluoro-4-methylquinazolin-6-yl)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide
반응식
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[C:19]([F:20])=[C:18]2[C:13]([C:14]([CH3:21])=[N:15][CH:16]=[N:17]2)=[CH:12][C:11]=1[NH:22][S:23]([C:26]1([CH2:29][CH2:30][O:31][Si](C(C)(C)C)(C)C)[CH2:28][CH2:27]1)(=[O:25])=[O:24].Cl>C1COCC1>[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[C:19]([F:20])=[C:18]2[C:13]([C:14]([CH3:21])=[N:15][CH:16]=[N:17]2)=[CH:12][C:11]=1[NH:22][S:23]([C:26]1([CH2:29][CH2:30][OH:31])[CH2:28][CH2:27]1)(=[O:24])=[O:25]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of N-(7-(2-fluoro-4-iodophenylamino)-8-fluoro-4-methylquinazolin-6-yl)-1-(2-(tert-butyldimethylsilyloxy)ethyl)cyclopropane-1-sulfonamide (36 mg, 0.056 mmol) in THF (2 ml) is added HCl (0.18 ml, 1.2 N in H2O, 0.22 mmol). After stirring for 1 h, the reaction is quenched with saturated aqueous NaHCO3 solution (3 ml) and extracted with EtOAc (2×10 ml). The combined organic solution is dried over Na2SO4 and concentrated. Silica gel chromatography yields the title compound.
후처리
- customthe reaction is quenched with saturated aqueous NaHCO3 solution (3 ml)
- extractionextracted with EtOAc (2×10 ml)
- dry with materialThe combined organic solution is dried over Na2SO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-1708dc68f5454cc097cc854747776c8d
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07820664B2
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