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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352247Generated: October 26, 2026

1,2-Dichloroethane → N-{[3-(9-Chloro-3-methyl-4-oxo-5H-isoxazolo[4,3-c]quinolin-5-yl) cyclohexylcarbamoyl]-methyl}-2-phenyl-acetamide

https://huagongshe.com/reaction/352247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantN-Benzylglycine HydrochlorideHCID 2756624—
Reactant5-(3-Aminocyclohexyl)-9-chloro-3-methyl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodideHCID 22713713—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductN-{[3-(9-Chloro-3-methyl-4-oxo-5H-isoxazolo[4,3-c]quinolin-5-yl) cyclohexylcarbamoyl]-methyl}-2-phenyl-acetamideHCID 22714202—

Reaction Steps

5-(3-Amino-cyclohexyl)-9-chloro-3-methyl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodide (70 mg, 0.19 mmol) was combined with EDC (47 mg, 0.25 mmol), 1-hydroxy-7-azabenzo-triazole (34 mg, 0.25 mmol), N,N-diisopropylethyl amine (0.10 mL, 0.58 mmol), DMAP (5 mg, cat.), and N-benzylglycine hydrochloride (50 mg, 0.25 mmol) in DMF(6 mL) and the mixture stirred overnight at rt. The mixture was then concentrated in vacuo and the residue taken up in chloroform/MeOH and the organic solution washed with aqueous NaHCO3. The organic solution was dried over Na2SO4 and concentrated in vacuo. The residue was loaded onto a silica gel column and eluted with MeOH/CH2Cl2, which allowed for the recovery of 32 mg (35%) of the free base. This material was dissolved in minimal EtOAc and treated with excess diethyl ether/hydrochloric acid. Concentration of this mixture to dryness allowed for quantitative recovery of the hydrochloride salt as an off white solid. MS(ES): (M+1)+ 479.1, 481.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743794B2
Source datasetuspto-grants-2004_06
ORD IDord-19d124634a7d4058a800422b47c9ed87
Source noteuspto-grants-2004_06