反应 #4164003
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-3b1d359464e14c73b735e4e539f6b6b7暂无可渲染的结构数据
CC(C)(C)OC(=O)NC1CCC2=CC=CC=C2NC1=O中间体产品
tert-butyl N-(2-oxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl)carbamate
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 | (2-氧-2,3,4,5-四氢-1H-苯并[B]氮杂卓-3-基)-氨基甲酸叔丁酯 |
|---|---|
| English name | tert-butyl N-(2-oxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl)carbamate |
| IUPAC 名称 | — |
| CAS号 | 86499-69-6 |
| 数据库编号 | 13243501 |
| 分子式 | — |
| 分子量 | — |
产品信息
(2-氧-2,3,4,5-四氢-1H-苯并[B]氮杂卓-3-基)-氨基甲酸叔丁酯(CAS 86499-69-6)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 13243501
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
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3b1d359464e14c73b735e4e539f6b6b7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ca57b5574fd4ead82267da3119e2e79反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07e50b7f8a26443db0b562df39f02714反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6aed3accba694148a5f7857b2606f18c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3b1d359464e14c73b735e4e539f6b6b7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-amino-2,3,4,5-tetrahydro-1H[1]benzazepin-2-one (4.0 g), 2-t-butyloxycarbonyloxyimino-2-phenylacetonitrile (6.1 g) and triethylamine (5 ml) in water (20 ml) and dioxane (25 ml) was stirred at room temperature for 18 hours. The resulting solid was filtered off and washed with water. Recrystallization from ethyl acetate gave 3-t-butyloxycarbonylamino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 199°-201°. The resulting solid was filtered off washed with water Recrystallization from ethyl acetate
来源 ID: ord-094ac74c660c422aadcfe28ba4a169be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-amino-2,3,4,5-tetrahydro-1H[1]benzazepin-2-one (4.0 g), 2-t-butyloxycarbonyloxyimino-2-phenylacetonitrile (6.1 g) and triethylamine (5 ml) in water (20 ml) and dioxane (25 ml) was stirred at room temperature for 18 hours. The resulting solid was filtered off and washed with water. Recrystallization from ethyl acetate gave 3-t-butyloxycarbonylamino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 199°-201°. The resulting solid was filtered off washed with water Recrystallization from ethyl acetate
来源 ID: ord-094ac74c660c422aadcfe28ba4a169be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-amino-2,3,4,5-tetrahydro-1H[1]benzazepin-2-one (4.0 g), 2-t-butyloxycarbonyloxyimino-2-phenylacetonitrile (6.1 g) and triethylamine (5 ml) in water (20 ml) and dioxane (25 ml) was stirred at room temperature for 18 hours. The resulting solid was filtered off and washed with water. Recrystallization from ethyl acetate gave 3-t-butyloxycarbonylamino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 199°-201°. The resulting solid was filtered off washed with water Recrystallization from ethyl acetate
来源 ID: ord-d2b0010bc2bf4f41acf908b3335decb9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ca57b5574fd4ead82267da3119e2e79反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07e50b7f8a26443db0b562df39f02714反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6aed3accba694148a5f7857b2606f18c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-amino-2,3,4,5-tetrahydro-1H[1]benzazepin-2-one (4.0 g), 2-t-butyloxycarbonyloxyimino-2-phenylacetonitrile (6.1 g) and triethylamine (5 ml) in water (20 ml) and dioxane (25 ml) was stirred at room temperature for 18 hours. The resulting solid was filtered off and washed with water. Recrystallization from ethyl acetate gave 3-t-butyloxycarbonylamino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, m.p. 199°-201°. The resulting solid was filtered off washed with water Recrystallization from ethyl acetate
来源 ID: ord-0872db8c849b4e49b871ed14452550d4PubChem 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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