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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914720Generated: October 31, 2026

Acetoxyacetyl chloride → HCID 59353085, compound

https://huagongshe.com/reaction/1914720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 3302617HCID 3302617—
SolventDichloromethaneHCID 6344—
ProductHCID 59353085HCID 5935308597.3%

Reaction Steps

To a suspension of 4-amino-N-(3-chloroquinoxalin-2-yl)benzenesulfonamide (2 g; 4.49 mmol; 1 eq) in DCM (100 mL) is added acetoxyacetyl chloride (1.23 mL; 9 mmol; 2 eq) and N-ethyldiisopropylamine (2.3 mL; 13.5 mmol; 3 eq) and the reaction mixture is stirred at room temperature for 30 min. DCM is removed under reduced pressure and the crude residue is dissolved in EtOAc. The organic phase is washed twice with 10% citric acid then brine. The solvent is evaporated and the residue is taken up in iPrOH then refluxed and left at room temperature until precipitation. The precipitate is filtered off then dried under reduced pressure to afford 1.9 g (95%) of the title compound as a yellow powder. 1H NMR (DMSO-d6) δ 10.70 (s, 1H), 8.25 (m, 2H), 8.09 (m, 4H), 7.88 (m, 2H), 4.71 (s, 2H), 2.13 (s, 3H). HPLC (max plot) 98%; Rt 4.03 min. UPLC/MS (ES+) 435.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614215B2
Source datasetuspto-grants-2013_12
ORD IDord-04eac3868a514b3892b927e53b360477
Source noteuspto-grants-2013_12