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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528538Generated: October 30, 2026

Trifluoroacetic acid → HCID 71711303, compound

https://huagongshe.com/reaction/528538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89761899HCID 89761899—
SolventDichloromethaneHCID 6344—
ProductHCID 71711303HCID 71711303—

Reaction Steps

4-Acetyl-1-(2-chloro-4-(trifluoromethyl)phenyl)-N-(2,4-dimethoxybenzyl)-N-(1,2,4-thiadiazol-5-yl)-1,2,3,4-tetrahydroquinoxaline-6-sulfonamide (0.048 g, 0.072 mmol) was dissolved in 1 mL of DCM and TFA (0.1 mL, 1.298 mmol) was added. The reaction was stirred for 30 minutes. The material was concentrated, dissolved in acetonitrile and loaded onto an ion exchange column (pre-wetted with acetonitrile). The column was flushed several times with acetonitrile, then the product was liberated by flushing the column several times with about 1M HCl solution in MeOH/EtOAc (made by adding acetyl chloride to a MeOH/EtOAc mixture). The second filtrate was concentrated to afford 4-acetyl-1-(2-chloro-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-yl)-1,2,3,4-tetrahydroquinoxaline-6-sulfonamide as a light pink solid. 1H NMR (400 MHz, DMSO-d6) δ=8.42 (s, 1 H), 8.12 (d, J=1.7 Hz, 1 H), 7.90 (dd, J=1.6, 8.4 Hz, 1 H), 7.81 (d, J=8.5 Hz, 1 H), 7.31 (d, J=7.9 Hz, 1 H), 6.21 (d, J=8.8 Hz, 1 H), 3.96 (t, J=4.6 Hz, 2 H), 3.68 (br. s., 2 H), 2.24 (s, 3 H). m/z (ESI) 517.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346798B2
Source datasetuspto-grants-2016_05
ORD IDord-caff288738144d5480456bd551388474
Source noteuspto-grants-2016_05