Hydrochloric Acid → 4-{[(2-Fluoro-4-hydroxy-6-methyl-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:33])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]([C:13]2[C:18]([CH3:19])=[CH:17][C:16]([O:20][Si](C(C)C)(C(C)C)C(C)C)=[CH:15][C:14]=2[F:31])[CH3:12])=[CH:6][C:5]=1[CH3:32].[F-].C([N+](CCCC)(CCCC)CCCC)CCC.Cl>C1COCC1>[CH3:1][O:2][C:3](=[O:33])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]([C:13]2[C:18]([CH3:19])=[CH:17][C:16]([OH:20])=[CH:15][C:14]=2[F:31])[CH3:12])=[CH:6][C:5]=1[CH3:32]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 0 °C
실험 절차
A mixture of 4-{[(2-fluoro-6-methyl-4-triisopropylsilanyloxy-phenyl)-methyl-amino]-methyl}-2-methyl-benzoic acid methyl ester (457 mg, 0.965 mmol) and tetrabutylammonium fluoride (2.0 mL of 1M in THF, 2.0 mmol) in THF (10 mL) is stirred at 0° C. for 20 minutes and then 2.0 mL of 1M HCl is added and the mixture is concentrated. The residue is portioned between ethyl acetate and brine. The layers are separated and the brine layer is extracted with ethyl acetate. The combined ethyl acetate layers are dried (MgSO4) and concentrated. The residue is purified on 40 g silica with ethyl acetate in heptane gradient (10% to 70%) to provide 233 mg (76%) of the titled compound as a glass. LC-ES/MS m/e 318.2 (M+1).
후처리
- concentrationthe mixture is concentrated
- customThe layers are separated
- extractionthe brine layer is extracted with ethyl acetate
- dry with materialThe combined ethyl acetate layers are dried (MgSO4)
- concentrationconcentrated
- customThe residue is purified on 40 g silica with ethyl acetate in heptane gradient (10% to 70%)
출처 및 근거
- ORD 기록
- ord-f2758d59b18d41259792b9ea7dad92b1
- 출처 데이터셋
- uspto-grants-2010_12
- 특허 번호
- US07846960B2
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