1-(2-Hydroxyethyl)piperazine → N-(7-Chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-nicotinamide

HRID 1887901Notes

Reaction equation

HRID 1887901 reaction equation
Cl[C:2]1[CH:29]=[CH:28][C:5]([C:6]([NH:8][CH2:9][C:10]2[C:19](=[O:20])[C:18]3[C:13](=[CH:14][C:15]([Cl:21])=[CH:16][CH:17]=3)[N:12]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:11]=2)=[O:7])=[CH:4][N:3]=1.[OH:30][CH2:31][CH2:32][N:33]1[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]1>>[Cl:21][C:15]1[CH:14]=[C:13]2[C:18]([C:19](=[O:20])[C:10]([CH2:9][NH:8][C:6](=[O:7])[C:5]3[CH:28]=[CH:29][C:2]([N:36]4[CH2:37][CH2:38][N:33]([CH2:32][CH2:31][OH:30])[CH2:34][CH2:35]4)=[N:3][CH:4]=3)=[CH:11][N:12]2[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)=[CH:17][CH:16]=1

Participants

3

Procedure

N-(7-Chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-nicotinamide was prepared starting from intermediate E and N-(2-hydroxyethyl)piperazine. MS calcd. for C28H28ClN5O3 [(M+H)+] 518.2, obsd. 518.0.

Sources & evidence

ORD record
ord-6fca3e96d92b4be78cc0918eedb005df
Source dataset
uspto-grants-2013_08
Patent number
US08501732B2

Reaction notes

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