Hydrochloric Acid → tert-Butyl ((4S,6S)-4-(5-bromo-2-fluoropyridin-3-yl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)carbamate
반응식
C([N:9]([C:17]1[O:18][C@H:19]([C:32]([F:35])([F:34])[F:33])[CH2:20][C@:21]([C:24]2[C:25]([F:31])=[N:26][CH:27]=[C:28]([Br:30])[CH:29]=2)([CH3:23])[N:22]=1)[C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])(=O)C1C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+].Cl>CO>[Br:30][C:28]1[CH:29]=[C:24]([C@:21]2([CH3:23])[CH2:20][C@@H:19]([C:32]([F:34])([F:33])[F:35])[O:18][C:17]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:14])([CH3:13])[CH3:15])=[N:22]2)[C:25]([F:31])=[N:26][CH:27]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
The crude product (5i) from step 7 was dissolved in MeOH (15 mL). Potassium carbonate (Aldrich, 0.200 g, 1.445 mmol) was added and the reaction was stirred at room temperature for 40 min. Hydrogen chloride (4M in 1,4-dioxane; 1.1 mL, 4.40 mmol) was added to the reaction mixture and the solvent was removed under the reduced pressure. The residue was diluted with EtOAc and water. The organic layer was washed with brine, and dried over sodium sulfate. The filtrate was concentrated and the residue used in the next step without further purification. MS m/z=400, 402 [M−tBu]+/[M+2−tBu]+; Calculated for C16H18BrF4N0O3: 456.2
후처리
- customthe solvent was removed under the reduced pressure
- additionThe residue was diluted with EtOAc and water
- washThe organic layer was washed with brine
- dry with materialdried over sodium sulfate
- concentrationThe filtrate was concentrated
- customthe residue used in the next step without further purification
출처 및 근거
- ORD 기록
- ord-a953261741fe48ceaa40ebc056d6010d
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09296734B2
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