Ethyl isocyanate → HCID 58979994, 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].[CH2:24]([N:26]=[C:27]=[O:28])[CH3:25]>>[CH2:24]([NH:26][C:27]([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:28])[CH3:25]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 ethyl isocyanate provided the title compound. ESMS [M+H]+: 375.2
Sources & evidence
- ORD record
- ord-319ae29bad8b46389286461cc8860217
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07419988B2
Reaction notes
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