反应 #4149221
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-2e26d34c1f5c437a90d617f3edcee0c7暂无可渲染的结构数据
CCCCCCCCCCOC(=O)Cl产品信息
氯甲酸(N-癸基)酯(CAS 55488-51-2)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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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-2e26d34c1f5c437a90d617f3edcee0c7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0fc9b7ce4c7347ff971ddb274b833a1d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-749f6cce9cfe4d96b1df7b437a29cd86反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af67c6c19e2446c08b82c79dd8640018反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-[2-[4-(1-decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-8b1a8c897ea84fea867612c5d9fbd265反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-[2-[4-(1 decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-dba503b1fab146918fa8d7f3b672c978反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-[2-[4-(1-decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-77281d25848f4f1792bc8b121e42c4bc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2e26d34c1f5c437a90d617f3edcee0c7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0fc9b7ce4c7347ff971ddb274b833a1d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate, (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl ]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-[2-[4-(1-decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-6c4b5d0539034f00a2bac55bb73d77d6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate, (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl ]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-[2-[4-(1-decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-6c4b5d0539034f00a2bac55bb73d77d6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of decanyl chloroformate (2.4 g, 11 mmol), and N-[2-[4-(6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide (3.9 g, 10 mmol) was warmed on the steam bath for 15 minutes. The reaction was allowed to cool to ambient temperature, and then ether was added to the residue. The resulting solid was filtered to afford N-2-[4-(1-decanoxy-6-fluoro-1 H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride. was warmed on the steam bath for 15 minutes The resulting solid was filtered
来源 ID: ord-d4603c96652a4ca4bb4ba9ead92539f7PubChem References
以下资料来自该化合物的公开数据库参考记录。
