HCID 67281584, 화합물 → HCID 67282784, 화합물
반응식
C([O:8][C:9]1[C:10](=[O:22])[CH:11]=[C:12]([CH:16]([OH:21])[C:17]([F:20])([F:19])[F:18])[N:13]([CH3:15])[CH:14]=1)C1C=CC=CC=1>CO.[Pd]>[OH:8][C:9]1[C:10](=[O:22])[CH:11]=[C:12]([CH:16]([OH:21])[C:17]([F:18])([F:19])[F:20])[N:13]([CH3:15])[CH:14]=1참가 물질
실험 절차
A mixture of 5-benzyloxy-1-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one (3.1 g, 9.9 mmol) and methanol (60 mL) was sonicated to give a clear solution. To the solution was added Pd/C (10 wt. %, dry basis, on activated carbon, wet, Degussa type E101 NE/W, 0.58 g). The debenzylation reaction was conducted in a Parr hydrogenator under an atmosphere of hydrogen pressurized to 50 psi. The reaction was completed within 20 min. The reaction mixture was diluted with MeOH (100 mL), sonicated for about 20 min. A CELITE™ bed was prepared on a sintered glass, and washed with 6M HCl (100 mL), followed by water (7×50 mL) and then methanol (2×50 mL) under suction. The reaction mixture was filtered through the pre-treated CELITE™ bed. The filtrate was collected and concentrated in vacuo to give 5-hydroxy-1-methyl-2-(2,2,2-trifluoro-1-hydroxy-ethyl)-1H-pyridin-4-one as a solid product (2.05 g, 92% yield, HPLC Method 1 (Example 24), RT=7.4 min, HPLC purity (peak percent area): 99.4% at λ=280 nm). 1H NMR (DMSO-d6+D2O) δ ppm: 7.50 (s, 1H), 6.50 (s, 1H), 5.37 (q, J=6.5 Hz, 1H), 3.67 (s, 3H); MS-ESI (m/z) 224.2 [M+1]+, 206.2, 155.2 (100%), 140.1, 126.1.
후처리
- customwas sonicated
- customto give a clear solution
- customThe debenzylation reaction
- customsonicated for about 20 min
- customA CELITE™ bed was prepared on a sintered glass
- washwashed with 6M HCl (100 mL)
- filtrationThe reaction mixture was filtered through the pre-treated CELITE™ bed
- customThe filtrate was collected
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-480a6393d46648dc8e442fce9f2901e3
- 출처 데이터셋
- uspto-grants-2014_03
- 특허 번호
- US08673943B2
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