2-Pyrrolidin-1-yl-isonicotinic acid → HCID 71208441, compound
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:26]2[CH:27]=[C:28]([CH:32]=[CH:33][N:34]=2)[C:29](O)=[O:30])[CH2:25][CH2:24][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:29](=[O:30])[C:28]3[CH:32]=[CH:33][N:34]=[C:26]([N:21]4[CH2:22][CH2:23][CH2:24][CH2:25]4)[CH:27]=3)=[CH:4][N:5]2[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[CH:10][CH:9]=1Participants
3
Procedure
N-(7-Chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-2-pyrrolidin-1-yl-iso-nicotinamide was prepared starting from intermediate D and 2-(pyrrolidin-1-yl)isonicotinic acid. MS calcd. for C26H24ClN4O2 [(M+H)+] 459.2, obsd. 459.0.
Sources & evidence
- ORD record
- ord-82de916d25a8449b9263e2a2bd98d92b
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501732B2
Reaction notes
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