반응식
C([C@@H:8]1COC(=O)[N:9]1[C:14](=[O:36])[C@H:15]([CH2:19][C:20]1[C:25]([Cl:26])=[CH:24][C:23]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:22][C:21]=1[Cl:35])[CH2:16]C=O)C1C=CC=CC=1.[NH:37]1[C:45]2[CH:44](N)[CH2:43][CH2:42][CH2:41][C:40]=2[CH:39]=[N:38]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl.C(#N)C>[CH2:28]([O:27][C:23]1[CH:22]=[C:21]([Cl:35])[C:20]([CH2:19][C@@H:15]2[CH2:16][CH2:8][N:9]([CH:44]3[C:45]4[NH:37][N:38]=[CH:39][C:40]=4[CH2:41][CH2:42][CH2:43]3)[C:14]2=[O:36])=[C:25]([Cl:26])[CH:24]=1)[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
Add a solution of (R)-4-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-(4-benzyloxy-2,6-dichloro-benzyl)-4-oxo-butyraldehyde, Preparation 38, (9.95 g, 18.9 mmol) in CH2Cl2 (300 mL) to a solution of 4,5,6,7-tetrahydro-1H-indazol-7-ylamine (2.60 g, 19.00 mmol) in acetonitrile (300 mL) and stir for 30 minutes at room temperature under N2. Add sodium triacetoxyborohydride (12.02 g, 56.9 mmol) to the reaction and stir for 72 hours. Remove the solvent in vacuo and extract solid with ethyl acetate, water and saturated NaHCO3. Dry the organic layer (Na2SO4), filter and concentrate under vacuum. Purify the residue by silica gel chromatography with a gradient of 0 to 10% methanol in CH2Cl2 to afford 2.53 g (28%) of the title compound. MS (m/z): 470 (M+).
후처리
- additionAdd
- stirringstir for 72 hours
- customRemove the solvent in vacuo
- extractionextract solid with ethyl acetate, water and saturated NaHCO3
- dry with materialDry the organic layer (Na2SO4)
- filtrationfilter
- concentrationconcentrate under vacuum
- customPurify the residue by silica gel chromatography with a gradient of 0 to 10% methanol in CH2Cl2
출처 및 근거
- ORD 기록
- ord-a7448ea71a5743dbafc3e9a0aab1a6db
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07981918B2
연결된 노트
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