反应 #4062261
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-1639159d29cb47629d1a321f6b3c90fc暂无可渲染的结构数据
CC(C)(CCN1CCOCC1)N产品信息
2-甲基-4-(吗啉-4-基)丁烷-2-胺(CAS 1263002-61-4)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。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1639159d29cb47629d1a321f6b3c90fc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ad00c81c8d314d4bbafea6621b5487b3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 5-cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 42 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine (Example 35 d) as starting materials, MS (EI): m/e=388.3 [M+H]+.
来源 ID: ord-9f3a01cc6f3e4d58a8210d6e826f4bd3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 5-cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 42 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine (Example 35 d) as starting materials, MS (EI): m/e=388.3 [M+H]+.
来源 ID: ord-9f3a01cc6f3e4d58a8210d6e826f4bd3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-cyclopropylmethoxy-5-pyrrolidin-1-yl-pyridine-2-carboxylic acid (Example 14 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine as starting materials, MS (EI): 417.2 [M+H]+.
来源 ID: ord-2413871998104976bc100122b9f3a6d3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Amino-3-methyl-1-morpholinobutan-1-one (0.55 g, 2.96 mmol) and borane in THF (1 M, 6 mL, 6 mmol) were mixed together. The mixture was stirred at room temperature overnight, another portion borane in THF (6 mL) was added and the mixture stirred for another day. Methanol (5 mL) was added and the solvent was removed in vacuo. Water (20 mL) was added and the mixture was extracted with ethyl acetate (3×20 mL). The LC-MS showed still product in the water phase which was now extracted with methylene chloride (2×20 mL). The organic phases were combined, dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give the crude product (0.09 g); MS (EI): m/e=173.2 [M+H]+. the mixture stirred for another day the solvent was removed in vacuo Water (20 mL) was added the mixture was extracted with ethyl acetate (3×20 mL) was now extracted with methylene chloride (2×20 mL) dried over anhydrous sodium sulfate the solvent was removed in vacuo
来源 ID: ord-4943f3b5706449bd9914a341b2f33dc4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 5-cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 42 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine (Example 35 d) as starting materials, MS (EI): m/e=388.3 [M+H]+.
来源 ID: ord-3f4b28d6f3ab4e1587a4e79a85486873反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-cyclopropylmethoxy-5-pyrrolidin-1-yl-pyridine-2-carboxylic acid (Example 14 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine as starting materials, MS (EI): 417.2 [M+H]+.
来源 ID: ord-5b540615315f47bfa4c220f9c5bfb8f1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was synthesized in analogy to Example 1, using 6-cyclopropylmethoxy-5-pyrrolidin-1-yl-pyridine-2-carboxylic acid (Example 14 a) and 1,1-dimethyl-3-morpholin-4-yl-propylamine as starting materials, MS (EI): 417.2 [M+H]+.
来源 ID: ord-5b540615315f47bfa4c220f9c5bfb8f1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Amino-3-methyl-1-morpholinobutan-1-one (0.55 g, 2.96 mmol) and borane in THF (1 M, 6 mL, 6 mmol) were mixed together. The mixture was stirred at room temperature overnight, another portion borane in THF (6 mL) was added and the mixture stirred for another day. Methanol (5 mL) was added and the solvent was removed in vacuo. Water (20 mL) was added and the mixture was extracted with ethyl acetate (3×20 mL). The LC-MS showed still product in the water phase which was now extracted with methylene chloride (2×20 mL). The organic phases were combined, dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give the crude product (0.09 g); MS (EI): m/e=173.2 [M+H]+. the mixture stirred for another day the solvent was removed in vacuo Water (20 mL) was added the mixture was extracted with ethyl acetate (3×20 mL) was now extracted with methylene chloride (2×20 mL) dried over anhydrous sodium sulfate the solvent was removed in vacuo
来源 ID: ord-05a0d710e1cc4b0d80df81d55b717d37反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1639159d29cb47629d1a321f6b3c90fc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ad00c81c8d314d4bbafea6621b5487b3PubChem References
以下资料来自该化合物的公开数据库参考记录。
