반응식
[C:1]([C:4]1[C:9]2[CH:10]=[CH:11][CH:12]=[C:13]([F:14])[C:8]=2[C:7](=[O:15])[O:6][C:5]=1[NH:16][C@@H:17]([CH:25]1[CH2:27][CH2:26]1)[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([F:24])[CH:19]=1)(=[O:3])[CH3:2].[OH-:28].[Na+]>O1CCCC1.CO>[CH:25]1([C@H:17]([NH:16][C:5]([CH:4]([C:9]2[CH:10]=[CH:11][CH:12]=[C:13]([F:14])[C:8]=2[C:7]([OH:6])=[O:15])[C:1](=[O:3])[CH3:2])=[O:28])[C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([F:24])[CH:19]=2)[CH2:27][CH2:26]1참가 물질
반응물 2
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 20 °C
실험 절차
4-Acetyl-3-{[(S)-cyclopropyl-(3-fluoro-phenyl)-methyl]-amino}-8-fluoro-2-benzopyran-1-one (14.30 g, 38.72 mmol) was dissolved in a mixture of tetrahydrofuran (50 mL) and methanol (50 mL) and placed on an ice/water bath with stirring. NaOH (1 M in H2O, 100 ml) was added and stirring continued for 1 hour. The cold bath removed and the mixture was allowed to warm to r.t. (20° C.) during 1 hour. The reaction mixture was poured into ice-water mixture (200 g+200 ml), followed by slow addition of 2 M aq. HCl (200 mL) and extracted with ethyl acetate (200 mL), washed with sat. aq. NaCl, dried (Na2SO4), filtered and evaporated to give the title compound (14.65 g, yield 97.7%) as a pale brown foam. The crude product was used in the next step without further purification. LC-MS (m/z) 388.3 (MH+); tR=1.2. 1H NMR (500 MHz, DMSO-d6): a mixture of tautomers and diastereoisomers. The following compounds were prepared analogously:
후처리
- customplaced on an ice/water bath
- stirringstirring
- customThe cold bath removed
- additionThe reaction mixture was poured into ice-water mixture (200 g+200 ml)
- additionfollowed by slow addition of 2 M aq. HCl (200 mL)
- extractionextracted with ethyl acetate (200 mL)
- washwashed with sat. aq. NaCl
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-a11b287a5cde45dfbb64df16b666c464
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08173639B2
연결된 노트
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