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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277798Generated: October 31, 2026

Acetonitrile → HCID 20554253, compound

https://huagongshe.com/reaction/1277798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantMethyl chloroformateHCID 6586—
Reactant4-MethylmorpholineHCID 7972—
Reactant6-(4-Aminophenyl)-1,2-dihydro-2-oxonicotinic acidHCID 12918956—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 20554253HCID 20554253—

Reaction Steps

Methyl chloroformate, 1.7 ml (20 mM), was added to a solution of 2.9 g (20 mM) of alpha-acetamidoisobutyic acid, 2.2 ml (20 mM) of N-methylmorpholine in 50 ml CH3CN at -15° C. The mixture was stirred at -20° C. to -10° C. for 1/2 hr and to it was added in a dropwise manner preformed silylated pyridone solution (by stirring a mixture of 2.3 g (10 mM) of the 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid, 3.84 ml (30 mM) of Me3SiCl, 4.2 ml (30 mM) of Et3N in 100 ml CH2Cl2 for 40 min) at -10° C. After the addition, the mixture was allowed to stir at 0° C. for 2 hrs and at room temperature for 12 hrs. To the resulting suspension was added 10 ml of isopropanol, stirred for 10 min, and the solids filtered, washed with MeOH, ether, dried to give 2.5 g of 6-[4-(N-acetyl-alpha-amino-isobutyrylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278681
Source datasetuspto-grants-1981_07
ORD IDord-5b54233982004201b26855239acb785e
Source noteuspto-grants-1981_07