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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598462Generated: October 30, 2026

4-Methylmorpholine → HCID 86618079, compound

https://huagongshe.com/reaction/598462

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant3-Amino-N-methylbenzamideHCID 676526—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 86618080HCID 86618080—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86618079HCID 8661807941%

Reaction Steps

To a solution of N-(4-chloro-3-((trifluoromethyl)phenyl)-N-(4-(3-methylcarbamoylphenyl)carboxyaminophenyl) urea (0.14 g, 0.48 mmol), 3-methylcarbamoylaniline (0.080 g, 0.53 mmol), HOBT-H2O (0.14 g, 1.07 mmol), and N-methylmorpholine (0.5 mL, 1.07 mmol) in DMF (3 mL) at 0° C. was added EDCI.HCl (0.10 g, 0.53 mmol). The resulting mixture was allowed to warm to room temp. and was stirred overnight. The resulting mixture was treated with water (10 mL), and extracted with EtOAc (25 mL). The organic phase was concentrated under reduced pressure. The resulting yellow solids were dissolved in EtOAc (3 mL) then filtered through a pad of silica gel (17 g, gradient from 70% EtOAc/30% hexane to 10% MeOH/90% EtOAc) to give N-(4-chloro-3-((trifluoromethyl)phenyl)-N-(4-(3-methylcarbamoylphenyl) carbamoylphenyl) urea as a white solid (0.097 g, 41%): mp 225-229; TLC (100% EtOAc) Rf 0.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897623B2
Source datasetuspto-grants-2011_03
ORD IDord-62a68754b6a641d29b965c95edb09591
Source noteuspto-grants-2011_03