Ammonium formate → Methyl {3-[(2R)-2-aminopropyl]phenyl}acetate
반응식
[CH3:1][O:2][C:3](=[O:23])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:11][C@H:12]([NH:14][C@@H](C2C=CC=CC=2)C)[CH3:13])[CH:6]=1.C([O-])=O.[NH4+]>C(O)C.[OH-].[OH-].[Pd+2]>[NH2:14][C@H:12]([CH3:13])[CH2:11][C:7]1[CH:6]=[C:5]([CH2:4][C:3]([O:2][CH3:1])=[O:23])[CH:10]=[CH:9][CH:8]=1참가 물질
실험 절차
A solution of methyl[3-((2R)-2-{[(1R)-1-phenyl-ethyl]-amino}-propyl)-phenyl]-acetate (Preparation 64) (13.65 g, 40.9 mmol) and ammonium formate (12.9 g, 204 mmol) in ethanol (200 ml) was heated at reflux in the presence of 20% of palladium hydroxide on charcoal (Pd(OH)2/C, 1.36 g). After 3 hours the reaction mixture was cooled to room temperature, filtered through arbocel and the filtrate concentrated in vacuo. The residue was partitioned between dichloromethane (200 ml) and 880 ammonia (100 ml) and the organic phase separated. The aqueous phase was extracted with further dichlorormethane (3×100 ml) and the combined organic extracts washed with brine (100 ml), dried (sodium sulfate) and reduced in vacuo to give the title compound (8.48 g) as a pale yellow oil. 1H NMR (400 MHz, CDCl3): δ=7.90-7.87 (2H, m), 7.38-7.34 (2H, m), 3.90 (3H, s), 3.26-3.17 (1H, m), 2.78-2.73 (1H, dd), 2.64-2.59 (1H, dd), 1.14-1.12 (3H, d) ppm. LRMS (electrospray): m/z [M+H]+ 194.
후처리
- filtrationfiltered through arbocel
- concentrationthe filtrate concentrated in vacuo
- customThe residue was partitioned between dichloromethane (200 ml) and 880 ammonia (100 ml)
- customthe organic phase separated
- extractionThe aqueous phase was extracted with further dichlorormethane (3×100 ml)
- washthe combined organic extracts washed with brine (100 ml)
- dry with materialdried (sodium sulfate)
출처 및 근거
- ORD 기록
- ord-31b7c1f81eb84b57b7c97787ab6e615a
- 출처 데이터셋
- uspto-grants-2009_12
- 특허 번호
- US07629358B2
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