Methanol → 2-[2-methyl-3-[4-[4-(trifluoromethyl)benzamido]benzyl]-1H-indol-1-yl]acetic acid
반응식
[CH3:1][C:2]1[N:3]([CH2:31][C:32]([O:34]CC)=[O:33])[C:4]2[C:9]([C:10]=1[CH2:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][C:19](=[O:30])[C:20]3[CH:25]=[CH:24][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:22][CH:21]=3)=[CH:14][CH:13]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.O.[OH-].[Li+].O1CCCC1.CO>O>[CH3:1][C:2]1[N:3]([CH2:31][C:32]([OH:34])=[O:33])[C:4]2[C:9]([C:10]=1[CH2:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][C:19](=[O:30])[C:20]3[CH:25]=[CH:24][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:22][CH:21]=3)=[CH:14][CH:13]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Into a dry reaction vessel, ethyl 2-[2-methyl-3-[4-[4-(trifluoromethyl)benzamido]benzyl]-1H-indol-1-yl]acetate (600 mg, 1.21 mmol), lithium hydroxide monohydrate (153 mg, 3.64 mmol), 10 mL tetrahydrofuran, 10 mL methanol, 10 mL water were weighed, and stirred at room temperature for 1 h. The reaction was monitored to be complete by TLC. The solvent was rotate evaporated. It was adjusted to pH=3-4 with 2 N HCl solution. It was filtered, and the filter cake was washed with 20 mL methanol to obtain the product 480 mg as a white solid, at a yield of 85.1%.
후처리
- customThe solvent was rotate evaporated
- filtrationIt was filtered
- washthe filter cake was washed with 20 mL methanol
출처 및 근거
- ORD 기록
- ord-66c8ed0cbd844bf5885023b30e8a7b6b
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09233098B2
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