2-(2H-1,2,3-Triazol-2-yl)benzoic acid → HCID 89559966, compound
Reaction equation
Cl.[N:2]1[N:3]([C:7]2[CH:8]=[C:9]([CH:17]=[CH:18][CH:19]=2)[CH2:10][C@@H:11]2[CH2:16][CH2:15][CH2:14][CH2:13][NH:12]2)[N:4]=[CH:5][CH:6]=1.[N:20]1[N:21]([C:25]2[CH:33]=[CH:32][CH:31]=[CH:30][C:26]=2[C:27](O)=[O:28])[N:22]=[CH:23][CH:24]=1>>[N:2]1[N:3]([C:7]2[CH:8]=[C:9]([CH:17]=[CH:18][CH:19]=2)[CH2:10][C@@H:11]2[CH2:16][CH2:15][CH2:14][CH2:13][N:12]2[C:27]([C:26]2[CH:30]=[CH:31][CH:32]=[CH:33][C:25]=2[N:21]2[N:22]=[CH:23][CH:24]=[N:20]2)=[O:28])[N:4]=[CH:5][CH:6]=1Participants
3
Procedure
The title compound was prepared from (S)-2-(3-[1,2,3]triazol-2-yl-benzyl)-piperidine hydrochloride and 2-(2H-1,2,3-triazol-2-yl)benzoic acid E-2 following the procedure described for B-28. LC-MS D: tR=0.91 min; [M+H]+=414.05.
Sources & evidence
- ORD record
- ord-d8f7a27439894c61b671a95c822b9d5b
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150566B2
Reaction notes
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