2-Chloro-1-(difluoromethoxy)-4-isocyanatobenzene → HCID 57445348, compound

HRID 550945Notes

Reaction equation

HRID 550945 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[CH:12][N:13]=[CH:14][CH:15]=3)[NH:10][C:9]=2[C:17]([NH2:19])=[O:18])=[CH:4][CH:3]=1.[Cl:20][C:21]1[CH:22]=[C:23]([N:31]=[C:32]=[O:33])[CH:24]=[CH:25][C:26]=1[O:27][CH:28]([F:30])[F:29]>>[Cl:20][C:21]1[CH:22]=[C:23]([NH:31][C:32](=[O:33])[NH:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[C:16]4[C:11](=[CH:12][N:13]=[CH:14][CH:15]=4)[NH:10][C:9]=3[C:17]([NH2:19])=[O:18])=[CH:6][CH:7]=2)[CH:24]=[CH:25][C:26]=1[O:27][CH:28]([F:30])[F:29]

Participants

3

Reactant 2

HCID 198528212-Chloro-1-(difluoromethoxy)-4-isocyanatobenzeneHCID 574453513-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide

Product 1

HCID 57445348HCID 57445348, compound

Procedure

93 mg of pale yellow solid 3-{4-[3-(3-chloro-4-difluoromethoxyphenyl)-ureido]phenyl}-1H-pyrrolo[2,3-c]pyridine-2-carboxamide are prepared as described in Example 1 starting with 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide and 3-chloro-4-difluoromethoxyphenyl isocyanate.

Sources & evidence

ORD record
ord-725e7b925b924e139951fe3d957dba1a
Source dataset
uspto-grants-2011_05
Patent number
US07947706B2

Reaction notes

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