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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984902Generated: November 2, 2026

Dimethylacetamide → HCID 178483093, compound

https://huagongshe.com/reaction/1984902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactant2-(Trifluoromethoxy)benzoyl ChlorideHCID 2777241—
ReactantHCID 178463885HCID 178463885—
SolventDichloromethaneHCID 6344—
ProductHCID 178483093HCID 17848309327.1%

Reaction Steps

To a suspension of polymer supported DMA (2.45 g, 7.35 mmol) in CH2Cl2 (6 mL) were added 2-trifluoromethoxy-benzoyl chloride (472 mg, 2.10 mmol) and cis-N2-(4-amino-cyclohexyl)-N4,N4-dimethylquiazoline-2,4-diamine obtained in step C of example 9 (300 mg, 1.05 mmol). The mixture was stirred at ambient temperature for 24 h, filtered, poured into saturated aqueous NaHCO3. The aqueous layer was extracted with CHCl3 (three times). The combined organic layer was dried over MgSO4, filtered, concentrated, purified by medium-pressure liquid chromatography (NH-silica gel, 25% EtOAc in hexane), and concentrated. To a solution of the residue in EtOAc (1 mL) was added 4 M hydrogen chloride in EtOAc (10 mL). The reaction mixture was stirred at ambient temperature for 1 hr, and concentrated. A solution of the residue in Et2O (10 mL) was stirred at ambient temperature for 1 hr and the precipitate was collected by filtration to give cis-N-[4-(4-dimethylaminoquinazolin-2-ylamino)-cyclohexyl]-2-trifluoromethoxy-benzamide hydrochloride (145 mg, 27%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544690B2
Source datasetuspto-grants-2009_06
ORD IDord-c6384320936c49d3a2964921a45a3162
Source noteuspto-grants-2009_06