Methylamine → 4-chloro-3-((trifluoromethyl)phenyl)-N'-(4-(3-methylcarbamoylphenyl) carboxyaminophenyl)urea

HRID 898977Notes

Reaction equation

HRID 898977 reaction equation
[Cl:1][C:2]1([C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([C:32](OC)=[O:33])[CH:27]=2)[CH:7]=[CH:6][C:5]([N:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:18]([F:21])([F:20])[F:19])[C:9](=[O:11])[NH2:10])=[C:4]([NH:22][C:23]([OH:25])=[O:24])[CH2:3]1.[CH3:36][NH2:37]>>[Cl:1][C:2]1([C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([C:32](=[O:33])[NH:37][CH3:36])[CH:27]=2)[CH:7]=[CH:6][C:5]([N:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:18]([F:19])([F:21])[F:20])[C:9](=[O:11])[NH2:10])=[C:4]([NH:22][C:23]([OH:25])=[O:24])[CH2:3]1

Participants

3

Procedure

To a sample of N-(4-chloro-3-((trifluoromethyl)phenyl)-N′-(4-(3-carbomethoxyphenyl) carboxyaminophenyl)urea (0.17 g, 0.34 mmol) was added methylamine (2 M in THF; 1 mL, 1.7 mmol) and the resulting mixture was stirred at room temp. overnight, then concentrated under reduced pressure to give N-(4-chloro-3-((trifluoromethyl)phenyl)-N′-(4-(3-methylcarbamoylphenyl)carboxyaminophenyl)urea as a white solid: mp 247; TLC (100% EtOAc) Rf 0.35.

Workup

  1. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-8b3a4bb0f0544b4488d75cb318acfa24
Source dataset
uspto-grants-2008_04
Patent number
US07351834B1

Reaction notes

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