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三乙酰氧基硼氢化钠 → HCID 67316393,化合物
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 三乙酰氧基硼氢化钠 | HCID 5049666 | — |
| 反应物 | 4,5,6,7-四氢-1H-吲唑-7-胺 | HCID 21941962 | — |
| 反应物 | (R)-4-((R)-benzyl-2-oxo-oxazolidin-3-yl)-3-(4-benzyloxy-2,6-dichloro-benzyl)-4-oxo-butyraldehyde | HCID 59515429 | — |
| 溶剂 | 乙腈 | HCID 6342 | — |
| 溶剂 | 二氯甲烷 | HCID 6344 | — |
| 产物 | HCID 67316393 | HCID 67316393 | 28% |
反应步骤
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+).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US07981918B2 |
| 来源数据集 | uspto-grants-2011_07 |
| ORD ID | ord-a7448ea71a5743dbafc3e9a0aab1a6db |
| 来源说明 | uspto-grants-2011_07 |