HCID 66928762, compound → HCID 66929134, compound
Reaction equation
[CH3:1][C:2]1([C:7]2[O:11][C:10]([CH2:12][N:13]3[CH:17]=[CH:16][C:15]([NH2:18])=[N:14]3)=[CH:9][CH:8]=2)[O:6]CCO1.[C:19]([O:23][C:24]([C:26]1[CH:27]=[C:28]([C:32]2[O:36][CH:35]=[N:34][C:33]=2[C:37](O)=[O:38])[CH:29]=[CH:30][CH:31]=1)=[O:25])([CH3:22])([CH3:21])[CH3:20]>>[C:19]([O:23][C:24](=[O:25])[C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([C:32]2[O:36][CH:35]=[N:34][C:33]=2[C:37](=[O:38])[NH:18][C:15]2[CH:16]=[CH:17][N:13]([CH2:12][C:10]3[O:11][C:7]([C:2](=[O:6])[CH3:1])=[CH:8][CH:9]=3)[N:14]=2)[CH:27]=1)([CH3:22])([CH3:20])[CH3:21]Participants
3
Procedure
Following general procedure B followed by C, starting from 1-[5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and 5-(3-tert-butoxycarbonyl-phenyl)-oxazole-4-carboxylic acid. LC-MS-conditions 02: tR=1.09 min; [M+H]+=477.45.
Sources & evidence
- ORD record
- ord-6ab64b1200a646428b2580f6c7fe0ad7
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288419B2
Reaction notes
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