1,3-Dioxaindane-4-carboxylic acid → HCID 67081332, compound
Reaction equation
[NH2:1][CH2:2][C@@H:3]1[CH2:8][C@H:7]2[C@H:5]([CH2:6]2)[N:4]1[C:9]([C:11]1[N:12]=[C:13]([CH3:23])[S:14][C:15]=1[C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[CH:17]=1)=[O:10].[O:24]1[C:28]2[CH:29]=[CH:30][CH:31]=[C:32]([C:33](O)=[O:34])[C:27]=2[O:26][CH2:25]1>>[F:22][C:18]1[CH:17]=[C:16]([C:15]2[S:14][C:13]([CH3:23])=[N:12][C:11]=2[C:9]([N:4]2[C@H:3]([CH2:2][NH:1][C:33]([C:32]3[C:27]4[O:26][CH2:25][O:24][C:28]=4[CH:29]=[CH:30][CH:31]=3)=[O:34])[CH2:8][C@H:7]3[C@@H:5]2[CH2:6]3)=[O:10])[CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
prepared by reaction of [(1S,3S,5S)-3-aminomethyl-2-aza-bicyclo[3.1.0]hex-2-yl]-[5-(3-fluoro-phenyl)-2-methyl-thiazol-4-yl]-methanone with benzo[1,3]dioxole-4-carboxylic acid. LC-MS (basic): tR=0.87 min; [M+H]+=480.1.
Sources & evidence
- ORD record
- ord-2874f91bee354e86823a98652a70ec8a
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288435B2
Reaction notes
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