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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237370Generated: October 30, 2026

Acetic Acid → HCID 25027942, compound

https://huagongshe.com/reaction/237370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloroquinoxalineHCID 16659—
Reactant3,5-DimethoxyanilineHCID 66301—
ReactantBenzenesulfonaMide, 4-(1-Methylethoxy)-HCID 17817955—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 25027942HCID 25027942—

Reaction Conditions

Temperature125 °C

Reaction Steps

A solution of 2,3-dichloroquinoxaline (2.0 mL, 0.38 M) was combined with K2CO3 (105 mg, 0.76 mmol) in a glass vial. A solution of 4-isopropoxybenzene sulfonamide (1.75 mL, 0.43 M) was added and the solution was stirred overnight at 125° C. After cooling, acetic acid (45 mL, 0.79 mmol) and 3,5-dimethoxyaniline (230 mg, 1.5 mmol) were added. The reaction mixture was stirred again at 125° C. overnight. Upon cooling, the reaction mixture was diluted with 8 mL of methanol and then 8 mL of water. The precipitate was collected by filtration and recrystallized from N,N-dimethylacetamide/water to give 45 mg of product. 1H-NMR (400 MHz, d6-DMSO): 12.16 (bs, 1H), 8.93 (s, 1H), 8.03 (d, 2H), 7.92 (bs, 1H), 7.56 (d, 1H), 7.36 (m, 4H), 7.07 (d, 2H), 6.24 (s, 1H), 4.72 (m, 1H), 3.76 (s, 6H), 1.27 (d, 6H); MS (EI) C25H26N4O5S: 495 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642584B2
Source datasetuspto-grants-2014_02
ORD IDord-9709c696ff404912ae63935a6b910980
Source noteuspto-grants-2014_02