Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101426Generated: October 26, 2026

4-Methylmorpholine → 4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamide

https://huagongshe.com/reaction/2101426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl AcetateHCID 8857—
Reactant2-(Trifluoromethyl)phenyl isocyanateHCID 16794—
ReactantN-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromideHCID 68830145—
SolventDimethylformamideHCID 6228—
Product4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamideHCID 68826663—

Reaction Steps

N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide, (61b), (100 mg) was dissolved in DMF (3 mL) prior to the addition of 4-methylmorpholine (0.13 mL) and 2-trifluoromethylphenyl isocyanate (0.05 mL). After stirring overnight, EtOAc was added and the solution was washed with 1N HCl. The EtOAc was dried, filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide (50 mg). MS found: (M+Na)+=564.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572813B2
Source datasetuspto-grants-2009_08
ORD IDord-c92447eb1daa46a6b672856b729141ae
Source noteuspto-grants-2009_08