反应 #4162035
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-80aecf69c2004e39a923ebf7645d6ab2暂无可渲染的结构数据
C1COCCN1CC2=C(C(=CC=C2)N)C(=O)NC3=CC=CC=C3中间体产品
2-amino-6-(morpholin-4-ylmethyl)-N-phenylbenzamide
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-氨基-6-(吗啉-4-基甲基)-N-苯甲酰胺 |
|---|---|
| English name | 2-amino-6-(morpholin-4-ylmethyl)-N-phenylbenzamide |
| IUPAC 名称 | — |
| CAS号 | 870280-78-7 |
| 数据库编号 | 59841062 |
| 分子式 | — |
| 分子量 | — |
产品信息
2-氨基-6-(吗啉-4-基甲基)-N-苯甲酰胺(CAS 870280-78-7)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 59841062
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-80aecf69c2004e39a923ebf7645d6ab2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-80aecf69c2004e39a923ebf7645d6ab2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-4c0af56c331c4182846d973cd8a7528d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-d73af6f848a148f0a175046931012ebb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-d73af6f848a148f0a175046931012ebb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-beeffb8356664316aa986813d0c0551f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-beeffb8356664316aa986813d0c0551f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-713b44d11a0d41b19e4fb06e902fb41f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-e9a8afdaa046413caa931f2c81433aa7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-ec89b186e48a42c285c2f513e4dcc9fb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-8d2e516049ff46c8800497f1bd8f9b29反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of compound 7 (0.3 g) and 10% Pd/C (30 mg) in methanol (35 mL) was stirred under hydrogen (1 atm) for 1.5 h. The mixture was filtered through a bed of CELITE® and the filtrate was concentrated to provide a yellow solid product, intermediate compound 2. ESI-MS m/z=312 (MH+). The mixture was filtered through a bed of CELITE® the filtrate was concentrated
来源 ID: ord-36ddfec62c5c43b5b011e1700c9dfe9bPubChem 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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