Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81882Generated: October 30, 2026

Acetoxyacetyl chloride → HCID 86626697, compound

https://huagongshe.com/reaction/81882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantHCID 86626699HCID 86626699—
SolventAcetonitrileHCID 6342—
ProductHCID 86626697HCID 86626697—

Reaction Conditions

Temperature5 °C

Reaction Steps

The solution of tert-butyl N-{2-[(3-amino-2-chloroquinolin-4-yl)amino]-1,1-dimethylethyl}carbamate in acetonitrile from Part C was cooled to 5° C. using an ice bath. A solution of acetoxyacetyl chloride (4.8 g, 35.1 mmol) in acetonitrile (20 mL) was added dropwise at a rate such that the temperature of the reaction mixture was maintained at 5° C. After the addition was complete the ice bath was removed and the reaction mixture was allowed to stir at ambient temperature for 5 hours. The reaction mixture was concentrated under reduced pressure to provide 16.7 g of N-{2-[(3-acetoxyacetylamino-2-chloroquinolin-4-yl)amino]-1,1-dimethylethyl}carbamate hydrochloride as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846710B2
Source datasetuspto-grants-2014_09
ORD IDord-be9758223451408bbcf820993d77e7c0
Source noteuspto-grants-2014_09