tert-Butyl isocyanate → HCID 58980071, compound
Reaction equation
[CH2:1]([N:3]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]3[NH:14][CH:15]=[CH:16][C:9]=23)[C:5]([C:17]2[CH:23]=[CH:22][C:20]([NH2:21])=[CH:19][CH:18]=2)=[N:4]1)[CH3:2].[C:24]([N:28]=[C:29]=[O:30])([CH3:27])([CH3:26])[CH3:25]>>[CH3:25][C:24]([NH:28][C:29]([NH:21][C:20]1[CH:22]=[CH:23][C:17]([C:5]2[C:6]([C:8]3[CH:13]=[CH:12][N:11]=[C:10]4[NH:14][CH:15]=[CH:16][C:9]=34)=[CH:7][N:3]([CH2:1][CH3:2])[N:4]=2)=[CH:18][CH:19]=1)=[O:30])([CH3:27])[CH3:26]Participants
3
Procedure
Following the procedure described in Example 1 with 4-[1-ethyl-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-3-yl]aniline and tert-butyl isocyanate provided the title compound. ESMS [M+H]+: 403.2
Sources & evidence
- ORD record
- ord-5160ff0570c449a08b941638480d6248
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07419988B2
Reaction notes
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