反应 #4134492
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-c508cd396d9447eda6ad0f656d6534f6暂无可渲染的结构数据
CN1CCC2=CC=CC=C2C(C1=O)N中间体产品
5-amino-3-methyl-2,5-dihydro-1H-3-benzazepin-4-one
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-氨基-3-甲基-1,3,4,5-四氢苯并[d]氮杂环庚烷-2-酮 |
|---|---|
| English name | 5-amino-3-methyl-2,5-dihydro-1H-3-benzazepin-4-one |
| IUPAC 名称 | — |
| CAS号 | 253324-91-3 |
| 数据库编号 | 21072565 |
| 分子式 | — |
| 分子量 | — |
产品信息
1-氨基-3-甲基-1,3,4,5-四氢苯并[d]氮杂环庚烷-2-酮(CAS 253324-91-3)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 21072565
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-c508cd396d9447eda6ad0f656d6534f6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-bf637b4b39a84a5dbbc3c37115ede5cd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c508cd396d9447eda6ad0f656d6534f6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c508cd396d9447eda6ad0f656d6534f6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-5f51040d4af6409caec81830084986b8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-5f51040d4af6409caec81830084986b8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-509dbc4aea9b46ad9894a5f6cb289d59反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-f342d3cc1f1f4f97a8cf5530b27f2908反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-2ce4b00b3cc54fc6bf92ff1ee11cfc0d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-1e589b6d8bf44381a79e27d3a3818061反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-1e589b6d8bf44381a79e27d3a3818061反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following General Procedure A above using N-(3,5-difluorophenylacetyl)-L-alanine (Example B) and 1-amino-3-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one, the title compound was prepared. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification was by flash chromatography using ethyl acetate as the eluant. The reaction was monitored by tlc on silica gel (Rf=0.15 in ethyl acetate) and purification
来源 ID: ord-111d412d7af94646aa7eeaacf071de8fPubChem References
以下资料来自该化合物的公开数据库参考记录。
询价
请提供目标规格、数量、交付地区及用途,CATO 团队将核对供应能力并回复。
