1-(5-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)ethanone → N-(2-((5-Acetylfuran-2-yl)methyl)-2H-1,2,3-triazol-4-yl)-5-(4-iodo-3-methylphenyl)-2-methyloxazole-4-carboxamide
Reaction equation
[NH2:1][C:2]1[CH:6]=[N:5][N:4]([CH2:7][C:8]2[O:12][C:11]([C:13](=[O:15])[CH3:14])=[CH:10][CH:9]=2)[N:3]=1.[I:16][C:17]1[CH:22]=[CH:21][C:20]([C:23]2[O:27][C:26]([CH3:28])=[N:25][C:24]=2[C:29](O)=[O:30])=[CH:19][C:18]=1[CH3:32]>>[C:13]([C:11]1[O:12][C:8]([CH2:7][N:4]2[N:3]=[C:2]([NH:1][C:29]([C:24]3[N:25]=[C:26]([CH3:28])[O:27][C:23]=3[C:20]3[CH:21]=[CH:22][C:17]([I:16])=[C:18]([CH3:32])[CH:19]=3)=[O:30])[CH:6]=[N:5]2)=[CH:9][CH:10]=1)(=[O:15])[CH3:14]Participants
3
Procedure
Following general procedure A, starting from 1-(5-((4-amino-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)ethanone and 5-(4-iodo-3-methylphenyl)-2-methyloxazole-4-carboxylic acid. LC-MS-conditions 02: tR=1.12 min; [M+H]+=549.20.
Sources & evidence
- ORD record
- ord-3df81de814f4492ba9685fe6cf474af2
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580831B2
Reaction notes
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