反应 #4126901
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-986372552d274cec81f70d145bac1117暂无可渲染的结构数据
CCC(CC)N1CCNCC1产品信息
1-(3-戊基)-哌嗪(CAS 373356-51-5)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-986372552d274cec81f70d145bac1117反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a6ebd296cdf9430d814022ed0cc6bd76反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d558389e51db4990b920e250ea2d72e1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-923120e23b264d31a143ee1c6d18ff72反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fa208fed275a42b88b8474dd54fb65fc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 1-(pentan-3-yl)piperazine. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.88 (t, J=7.33 Hz, 6 H) 1.29 (dt, J=14.08, 6.98 Hz, 2 H) 1.47 (dt, J=14.08, 6.98 Hz, 2 H) 2.26 (t, J=6.57 Hz, 1 H) 2.43 (s, 3 H) 2.56 (br. s., 4 H) 3.37-3.48 (m, 2 H) 3.62 (br. s., 2 H) 7.64 (dd, J=8.08, 1.52 Hz, 1 H) 7.71 (s, 1 H) 7.82 (d, J=8.08 Hz, 1 H) 8.05 (dd, J=8.59, 2.27 Hz, 1 H) 8.12 (s, 1 H) 8.39 (d, J=8.59 Hz, 1 H) 8.53 (d, J=2.27 Hz, 1 H) 12.82 (br. s., 1 H); ESI-MS m/z [M+H]+ 459.3.
来源 ID: ord-bf805ca4b3ac49bb894e0fb592a99a0d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 1-(pentan-3-yl)piperazine. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.88 (t, J=7.33 Hz, 6H) 1.29 (dt, J=14.08, 6.98 Hz, 2H) 1.47 (dt, J=14.08, 6.98 Hz, 2H) 2.26 (t, J=6.57 Hz, 1H) 2.43 (s, 3H) 2.56 (br. s., 4H) 3.37-3.48 (m, 2H) 3.62 (br. s., 2H) 7.64 (dd, J=8.08, 1.52 Hz, 1H) 7.71 (s, 1H) 7.82 (d, J=8.08 Hz, 1H) 8.05 (dd, J=8.59, 2.27 Hz, 1H) 8.12 (s, 1H) 8.39 (d, J=8.59 Hz, 1H) 8.53 (d, J=2.27 Hz, 1H) 12.82 (br. s., 1H); ESI-MS m/z [M+H]+ 459.3.
来源 ID: ord-5b650bae391d4806a96af9f3a40200ea反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-986372552d274cec81f70d145bac1117反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a6ebd296cdf9430d814022ed0cc6bd76反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d558389e51db4990b920e250ea2d72e1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fa208fed275a42b88b8474dd54fb65fc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared by a similar procedure to that described in Example 23, starting from 4-[5-(4-(chloromethyl)phenyl)-[1,2,4]oxadiazol-3-ylmethyl]-1-(1-ethylpropyl)piperidine and 1-(1-ethylpropyl)piperazine. HPLC: Rt=6.50 min.
来源 ID: ord-8aac8451abf848289860a2d3c2505808PubChem References
以下资料来自该化合物的公开数据库参考记录。
