4-Carboxy-1,2,3-triazole → HCID 178483290, compound
Reaction equation
[NH:1]1[CH:5]=[C:4]([C:6]([OH:8])=O)[N:3]=[N:2]1.[CH3:9][NH:10][CH2:11][CH2:12][CH:13]1[CH2:18][CH2:17][N:16]([C:19]([O:21][CH2:22][C:23]2[CH:28]=[C:27]([Cl:29])[CH:26]=[C:25]([Cl:30])[CH:24]=2)=[O:20])[CH2:15][CH2:14]1>>[CH3:9][N:10]([CH2:11][CH2:12][CH:13]1[CH2:14][CH2:15][N:16]([C:19]([O:21][CH2:22][C:23]2[CH:24]=[C:25]([Cl:30])[CH:26]=[C:27]([Cl:29])[CH:28]=2)=[O:20])[CH2:17][CH2:18]1)[C:6]([C:4]1[N:3]=[N:2][NH:1][CH:5]=1)=[O:8]Participants
3
Procedure
The title compound was prepared analogously to Example 34, step 3 from 1H-1,2,3-triazole-4-carboxylic acid and 3,5-dichlorobenzyl 4-(2-(methylamino)ethyl)piperidine-1-carboxylate (Example 1, step 3) (200 mg, 0.579 mmol);
Sources & evidence
- ORD record
- ord-a4e683597f154ca5b2925ad48f5eee83
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409895B2
Reaction notes
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