6-Morpholinonicotinic Acid → N-(7-Chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-6-morpholin-4-yl-nicotinamide

HRID 1887865

Reaction equation

HRID 1887865 reaction equation
[NH2:1][CH2:2][C:3]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][C:8]([Cl:14])=[CH:9][CH:10]=2)[N:5]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:4]=1.[N:21]1([C:27]2[CH:35]=[CH:34][C:30]([C:31](O)=[O:32])=[CH:29][N:28]=2)[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>>[Cl:14][C:8]1[CH:7]=[C:6]2[C:11]([C:12](=[O:13])[C:3]([CH2:2][NH:1][C:31](=[O:32])[C:30]3[CH:34]=[CH:35][C:27]([N:21]4[CH2:22][CH2:23][O:24][CH2:25][CH2:26]4)=[N:28][CH:29]=3)=[CH:4][N:5]2[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[CH:10][CH:9]=1

Participants

3

Procedure

N-(7-Chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-6-morpholin-4-yl-nicotinamide was prepared starting from intermediate D and 6-morpholin-4-yl-nicotinic acid. MS calcd. for C26H23ClN4O3 [(M+H)+] 474.9, obsd. 474.9.

Sources & evidence

ORD record
ord-7b1bd0cde79a4a67b2d5dab5ebc64f35
Source dataset
uspto-grants-2013_08
Patent number
US08501732B2

Linked notes

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