6-Methyl-5-phenylpyridin-2-amine → 1-(2-Bromobenzoyl)-3-(6-methyl-5-phenyl-2-pyridyl)urea

HRID 1980334Notes

Reaction equation

HRID 1980334 reaction equation
[Br:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([N:6]=[C:7]=[O:8])=[O:5].[CH3:13][C:14]1[N:19]=[C:18]([NH2:20])[CH:17]=[CH:16][C:15]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(OCC)(=O)C>[Br:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([NH:6][C:7]([NH:20][C:18]1[CH:17]=[CH:16][C:15]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[C:14]([CH3:13])[N:19]=1)=[O:8])=[O:5]

Participants

4

Reactant 2

HCID 135028556-Methyl-5-phenylpyridin-2-amineHCID 146268852-Bromobenzoyl isocyanate

Product 1

HCID 132426561-(2-Bromobenzoyl)-3-(6-methyl-5-phenyl-2-pyridyl)urea

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

2-Bromobenzoyl isocyanate (650 mg) is reacted with 6-methyl-5-phenyl-2-pyridylamine (500 mg) in 25 ml of ethyl acetate. A precipitate forms which upon filtering constitutes the desired product.

Workup

  1. filtrationA precipitate forms which upon filtering

Sources & evidence

ORD record
ord-080032d53a914d3db37657f1dd4a9fbc
Source dataset
uspto-grants-1985_04
Patent number
US04508722

Reaction notes

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