Hydrochloric Acid → 3-{4-[(4-{[(4-Isopropyl-1,3-thiazol-2-yl)(3-methylbutyl)amino]methyl}benzyl)oxy]phenyl}propanoic acid
반응식
[CH:1]([C:4]1[N:5]=[C:6]([N:9]([CH2:15][C:16]2[CH:35]=[CH:34][C:19]([CH2:20][O:21][C:22]3[CH:27]=[CH:26][C:25]([CH2:28][CH2:29][C:30]([O:32]C)=[O:31])=[CH:24][CH:23]=3)=[CH:18][CH:17]=2)[CH2:10][CH2:11][CH:12]([CH3:14])[CH3:13])[S:7][CH:8]=1)([CH3:3])[CH3:2].O.Cl>CO.O1CCCC1.[OH-].[Na+]>[CH:1]([C:4]1[N:5]=[C:6]([N:9]([CH2:15][C:16]2[CH:17]=[CH:18][C:19]([CH2:20][O:21][C:22]3[CH:23]=[CH:24][C:25]([CH2:28][CH2:29][C:30]([OH:32])=[O:31])=[CH:26][CH:27]=3)=[CH:34][CH:35]=2)[CH2:10][CH2:11][CH:12]([CH3:14])[CH3:13])[S:7][CH:8]=1)([CH3:2])[CH3:3]참가 물질
7
반응물 3
생성물 1
시약·촉매·용매 3
실험 절차
Methyl 3-{4-[(4-{[(4-isopropyl-1,3-thiazol-2-yl)(3-methylbutyl)amino]methyl}benzyl)oxy]phenyl}propanoate (140 mg) was dissolved in a mixed solvent of methanol (2 mL) and tetrahydrofuran (2 mL), and 2N aqueous sodium hydroxide solution (2 mL) was added. The mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, acidified with 1N aqueous hydrochloric acid solution, and extracted with ethyl acetate. The ethyl acetate layer was dried using Presep Dehydration tube (manufactured by Wako Pure Chemical Industries, Ltd.), and concentrated to give the title compound (120 mg, yield 88%) as a pale-yellow oil.
후처리
- additionwas added
- extractionextracted with ethyl acetate
- dry with materialThe ethyl acetate layer was dried
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-f348630301544a0b8549e069dd629342
- 출처 데이터셋
- uspto-grants-2011_06
- 특허 번호
- US07960369B2
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