Methanesulfonic Acid → 3-(2-fluoro-4-{[4-({5-(2-phenylethyl)-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-1-yl}methyl)benzyl]amino}phenyl)propanoic acid methanesulfonate
반응식
[F:1][C:2]1[CH:7]=[C:6]([NH:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][N:17]3[C:21]([CH2:22][CH2:23][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)=[CH:20][C:19]([C:30]4[CH:35]=[CH:34][C:33]([C:36]([F:39])([F:38])[F:37])=[CH:32][CH:31]=4)=[N:18]3)=[CH:12][CH:11]=2)[CH:5]=[CH:4][C:3]=1[CH2:40][CH2:41][C:42]([OH:44])=[O:43].[CH3:45][S:46]([OH:49])(=[O:48])=[O:47]>C(OCC)(=O)C>[CH3:45][S:46]([OH:49])(=[O:48])=[O:47].[F:1][C:2]1[CH:7]=[C:6]([NH:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][N:17]3[C:21]([CH2:22][CH2:23][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)=[CH:20][C:19]([C:30]4[CH:31]=[CH:32][C:33]([C:36]([F:38])([F:37])[F:39])=[CH:34][CH:35]=4)=[N:18]3)=[CH:12][CH:11]=2)[CH:5]=[CH:4][C:3]=1[CH2:40][CH2:41][C:42]([OH:44])=[O:43]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 3-(2-fluoro-4-{[4-({5-(2-phenylethyl)-3-[4-(trifluoromethyl)phenyl]-1H-pyrazol-1-yl}methyl)benzyl]amino}phenyl)propanoic acid (500 mg, 0.83 mmol) in ethyl acetate (20 mL) was added methanesulfonic acid (95 mg, 1.0 mmol) at room temperature, and the mixture was stirred for 1 hr. The reaction mixture was concentrated, isopropyl ether was added and the precipitated crystals were collected by filtration, washed with isopropyl ether and dried to give the title compound as colorless crystals (348 mg, yield 60%).
후처리
- concentrationThe reaction mixture was concentrated
- additionisopropyl ether was added
- filtrationthe precipitated crystals were collected by filtration
- washwashed with isopropyl ether
- customdried
출처 및 근거
- ORD 기록
- ord-34d00a36266347b39c113dfdcddfa1ea
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07786165B2
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