反应 #4030050
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-817cc945933e4bc0951b91ec433675a3暂无可渲染的结构数据
CC(C)(C)OC(=O)N1CCCCCC1C(=O)O中间体产品
1-[(2-methylpropan-2-yl)oxycarbonyl]azepane-2-carboxylic acid
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 1-BOC-氮杂卓-2-甲酸 |
|---|---|
| English name | 1-[(2-methylpropan-2-yl)oxycarbonyl]azepane-2-carboxylic acid |
| IUPAC 名称 | — |
| CAS号 | 1034708-26-3 |
| 数据库编号 | 3292084 |
| 分子式 | — |
| 分子量 | — |
产品信息
1-BOC-氮杂卓-2-甲酸(CAS 1034708-26-3)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 3292084
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-817cc945933e4bc0951b91ec433675a3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phosphorus oxychloride (0.88 g, 5.73 mmol) is added drop wise at 0° C. to a solution of perhydro-azepine-1,2-dicarboxylic acid 1-tert-butyl ester (0.93 g, 3.82 mmol) and 5-tert-butyl-isoxazol-3-ylamine (0.54 g, 3.82 mol) in pyridine (10.0 mL). The reaction mixture is slowly warmed up to room temperature and stirred for three hours. The mixture is diluted with EtOAc and washed twice with saturated NH4Cl solution. The organic phase is washed with 1N HCl, and after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure to afford the crude product that is used in the next step without further purification; m/z 366 [M+H+]. washed twice with saturated NH4Cl solution The organic phase is washed with 1N HCl after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure
来源 ID: ord-f0789df63a734aff9ebb4ba04e0e9687反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phosphorus oxychloride (0.88 g, 5.73 mmol) is added drop wise at 0° C. to a solution of perhydro-azepine-1,2-dicarboxylic acid 1-tert-butyl ester (0.93 g, 3.82 mmol) and 5-tert-butyl-isoxazol-3-ylamine (0.54 g, 3.82 mol) in pyridine (10.0 mL). The reaction mixture is slowly warmed up to room temperature and stirred for three hours. The mixture is diluted with EtOAc and washed twice with saturated NH4Cl solution. The organic phase is washed with 1N HCl, and after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure to afford the crude product that is used in the next step without further purification; m/z 366 [M+H+]. washed twice with saturated NH4Cl solution The organic phase is washed with 1N HCl after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure
来源 ID: ord-f0789df63a734aff9ebb4ba04e0e9687反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phosphorus oxychloride (0.88 g, 5.73 mmol) is added drop wise at 0° C. to a solution of perhydro-azepine-1,2-dicarboxylic acid 1-tert-butyl ester (0.93 g, 3.82 mmol) and 5-tert-butyl-isoxazol-3-ylamine (0.54 g, 3.82 mol) in pyridine (10.0 mL). The reaction mixture is slowly warmed up to room temperature and stirred for three hours. The mixture is diluted with EtOAc and washed twice with saturated NH4Cl solution. The organic phase is washed with 1N HCl, and after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure to afford the crude product that is used in the next step without further purification; m/z 366 [M+H+]. washed twice with saturated NH4Cl solution The organic phase is washed with 1N HCl after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure
来源 ID: ord-f0789df63a734aff9ebb4ba04e0e9687反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-817cc945933e4bc0951b91ec433675a3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phosphorus oxychloride (0.88 g, 5.73 mmol) is added drop wise at 0° C. to a solution of perhydro-azepine-1,2-dicarboxylic acid 1-tert-butyl ester (0.93 g, 3.82 mmol) and 5-tert-butyl-isoxazol-3-ylamine (0.54 g, 3.82 mol) in pyridine (10.0 mL). The reaction mixture is slowly warmed up to room temperature and stirred for three hours. The mixture is diluted with EtOAc and washed twice with saturated NH4Cl solution. The organic phase is washed with 1N HCl, and after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure to afford the crude product that is used in the next step without further purification; m/z 366 [M+H+]. washed twice with saturated NH4Cl solution The organic phase is washed with 1N HCl after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure
来源 ID: ord-f0789df63a734aff9ebb4ba04e0e9687PubChem References
以下资料来自该化合物的公开数据库参考记录。
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