8-Quinolinecarboxylic acid → HCID 86653690, compound

HRID 2064899Notes

Reaction equation

HRID 2064899 reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([F:23])[CH:18]=2)=[C:5]([C:7]([N:9]2[C@H:14]([CH2:15][NH2:16])[CH2:13][C@H:12]3[C@@H:10]2[CH2:11]3)=[O:8])[N:6]=1.[N:24]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][C:32]=2[C:34](O)=[O:35])[CH:27]=[CH:26][CH:25]=1>>[NH2:1][C:2]1[S:3][C:4]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([F:23])[CH:18]=2)=[C:5]([C:7]([N:9]2[C@H:14]([CH2:15][NH:16][C:34]([C:32]3[CH:31]=[CH:30][CH:29]=[C:28]4[C:33]=3[N:24]=[CH:25][CH:26]=[CH:27]4)=[O:35])[CH2:13][C@H:12]3[C@@H:10]2[CH2:11]3)=[O:8])[N:6]=1

Participants

3

Procedure

prepared by reaction of [2-amino-5-(3-fluoro-phenyl)-thiazol-4-yl]-((1S,3S,5S)-3-aminomethyl-2-aza-bicyclo[3.1.0]hex-2-yl)-methanone with quinoline-8-carboxylic acid. LC-MS (basic): tR=0.82 min; [M+H]+=488.2.

Sources & evidence

ORD record
ord-afad88c0f8cd4976a81a9079e5d17b69
Source dataset
uspto-grants-2012_10
Patent number
US08288435B2

Reaction notes

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