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HRID 1013819生成日期:2026年10月23日

三乙酰氧基硼氢化钠 → HCID 67316393,化合物

https://huagongshe.com/zh-CN/reaction/1013819

反应方程式

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-butyraldehydeHCID 59515429—
溶剂乙腈HCID 6342—
溶剂二氯甲烷HCID 6344—
产物HCID 67316393HCID 6731639328%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07981918B2
来源数据集uspto-grants-2011_07
ORD IDord-a7448ea71a5743dbafc3e9a0aab1a6db
来源说明uspto-grants-2011_07