Methyl 2-(3,4,5-trimethoxyphenyl)acetate → HCID 135430917, compound
Reaction equation
[NH2:1][C:2]1[N:6]([CH:7]([CH:17]([OH:19])[CH3:18])[CH2:8][CH2:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:5]=[N:4][C:3]=1[C:20]([NH2:22])=[O:21].[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH2:35][C:36](OC)=O)[CH:28]=[C:29]([O:33][CH3:34])[C:30]=1[O:31][CH3:32]>>[CH3:34][O:33][C:29]1[CH:28]=[C:27]([CH:26]=[C:25]([O:24][CH3:23])[C:30]=1[O:31][CH3:32])[CH2:35][C:36]1[NH:22][C:20](=[O:21])[C:3]2[N:4]=[N:5][N:6]([CH:7]([CH:17]([OH:19])[CH3:18])[CH2:8][CH2:9][CH2:10][C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:2]=2[N:1]=1Participants
3
Procedure
Analogously to the procedure of Example XI, the title compound is prepared from 10 mg (0.024 mmol) of 5-amino-1-[1-(1-hydroxy-ethyl)-4-phenyl-butyl]-1H-[1,2,3]triazole-4-carboxamide and 20 mg (0.107 mmol) of methyl 3,4,5-trimethoxyphenylacetate.
Sources & evidence
- ORD record
- ord-0f7558b135be47d0a4fbff00b79f3984
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06458796B1
Reaction notes
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