反应 #3860377
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-b66c674976ea4f76bd563f55920d5b29暂无可渲染的结构数据
CCCN(CCC)CC1CCCCN1CCN中间体产品
N-[[1-(2-aminoethyl)piperidin-2-yl]methyl]-N-propylpropan-1-amine
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 | N-[[1-(2-氨基乙基)哌啶-2-基]甲基]-N-丙基丙-1-胺 |
|---|---|
| English name | N-[[1-(2-aminoethyl)piperidin-2-yl]methyl]-N-propylpropan-1-amine |
| IUPAC 名称 | — |
| CAS号 | 118289-11-5 |
| 数据库编号 | 10868438 |
| 分子式 | — |
| 分子量 | — |
产品信息
N-[[1-(2-氨基乙基)哌啶-2-基]甲基]-N-丙基丙-1-胺(CAS 118289-11-5)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 10868438
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
10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b66c674976ea4f76bd563f55920d5b29反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 11-(chlorocarbonyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and (+)-2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethanamine in a yield of 60% of theory. Colourless crystals, m.p. 164°-165° C. (acetonitrile); [α]D20 =+7.24° (dilute aqueous hydrochloric acid).
来源 ID: ord-911fa773a1f743cf9bab84c0e5186095反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 1 from 11-(chlorocarbonyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and (-)-2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethanamine in a yield of 90% of theory. Colourless crystals, m.p. 164°-165° C. (acetonitrile); [α]D20 =-7.62° (dilute aqueous hydrochloric acid).
来源 ID: ord-9bcbb34f405e4f28a7507088e2acf3f1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 1 from 6-chloro-5-(chlorocarbonyl)-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one and 2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethanamine in a yield of 2.6% of theory. Colourless crystals, m.p. 71°-78° C., presumably a mixture of 2 diastereomers. Colourless crystals, m.p. 71°-78° C., presumably a mixture of 2 diastereomers
来源 ID: ord-f91c1ce1c6c44b27802c2e9c4ecdd2ec反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 3-chloro-4-(chlorocarbonyl)-1-methyl-1,4,9,10-tetrahydro-pyrrolo[3,2-b][1,5]benzodiazepin-10-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 57% of theory.
来源 ID: ord-aadfe372169f48808dbee992001a9241反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 11-(chlorocarbonyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-5-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 66% of theory. Colourless crystals, m.p. 149°-151° C. (acetonitrile).
来源 ID: ord-0d53aea3b4ac432fb0c89643d57a42f2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 11-(chlorocarbonyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-5-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 66% of theory. Colourless crystals, m.p. 149°-151° C. (acetonitrile).
来源 ID: ord-0d53aea3b4ac432fb0c89643d57a42f2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 1 from 11-(chlorocarbonyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 87% of theory. Colourless crystals, m.p. 197°-199° C., not readily soluble in water.
来源 ID: ord-86f296ca73674e5fa1632ddd2a753d48反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 11-(chlorocarbonyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 88% of theory. Colourless crystals, m.p. 165° C. (acetonitrile).
来源 ID: ord-bcd4dcd613cb4c9b90533e97e9c8dc9f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared analogously to Example 2 from 11-(chlorocarbonyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and 2-[2-[(dipropylamino)methyl]-piperidin-1-yl]ethanamine in a yield of 88% of theory. Colourless crystals, m.p. 165° C. (acetonitrile).
来源 ID: ord-bcd4dcd613cb4c9b90533e97e9c8dc9fPubChem 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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