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【结 构 式】

【分子编号】28967

【品名】N-(3-chloropropyl)-N-isopropylamine

【CA登记号】

【 分 子 式 】C6H14ClN

【 分 子 量 】135.6366

【元素组成】C 53.13% H 10.4% Cl 26.14% N 10.33%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(II)

The condensation of 9-cyanofluorene (I) with 3-(dimethylamino)propyl chloride (II) by means of sodium amide in refluxing THF gives 9-[3-(dimethyl amino)propyl]-9-cyanofluorene (III), which is hydrolyzed partially with hot sulfuric acid water.

1 Wiegand, H.; Bosslet, S.; Bosslet, K.; Sedlacek, K. (Behringwerke AG); Neoglucoproteins, their preparation and use. AU 8944368; EP 0368131 .
2 Lacefield, W.B.; Simon R.L. (Eli Lilly and Company); Antiarrhythmic method. US 4197313 .
3 Serradell, M.N.; Sneddon, J.; Castaner, J.; Indecainide. Drugs Fut 1985, 10, 2, 121.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 28966 9H-fluorene-9-carbonitrile C14H9N 详情 详情
(II) 28967 N-(3-chloropropyl)-N-isopropylamine C6H14ClN 详情 详情
(III) 28968 9-[3-(isopropylamino)propyl]-9H-fluorene-9-carbonitrile C20H22N2 详情 详情
Extended Information