m-Tolyl isocyanate → HCID 57445307, compound

HRID 550915Notes

Reaction equation

HRID 550915 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[N:12][CH:13]=[CH:14][CH:15]=3)[NH:10][C:9]=2[C:17]([NH2:19])=[O:18])=[CH:4][CH:3]=1.[C:20]1([CH3:29])[CH:25]=[CH:24][CH:23]=[C:22]([N:26]=[C:27]=[O:28])[CH:21]=1>>[C:20]1([CH3:29])[CH:25]=[CH:24][CH:23]=[C:22]([NH:26][C:27](=[O:28])[NH:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[C:16]4[C:11](=[N:12][CH:13]=[CH:14][CH:15]=4)[NH:10][C:9]=3[C:17]([NH2:19])=[O:18])=[CH:6][CH:7]=2)[CH:21]=1

Participants

3

Procedure

62.5 mg of solid beige-coloured 3-[4-(3-m-tolylureido)phenyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxamide are prepared as described in Example 7 starting with 3-(4-aminophenyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxamide and m-tolyl isocyanate.

Sources & evidence

ORD record
ord-debc4807e6c14221b0316141add0d23f
Source dataset
uspto-grants-2011_05
Patent number
US07947706B2

Reaction notes

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