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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045942Generated: November 1, 2026

1,2-Dichloroethane → HCID 46916507, compound

https://huagongshe.com/reaction/2045942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant3-(2-Quinoxalinyl)anilineHCID 807264—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-Sulfamoylpropanoic acidHCID 21718767—
SolventDimethylformamideHCID 6228—
ProductHCID 46916507HCID 4691650740%

Reaction Steps

To a solution of (3-quinoxalin-2-ylphenyl)amine (120 mg, 0.545 mol) and 3-sulfamoylpropanoic acid (100 mg, 0.654 mmol) in dry DMF (3 mL), EDC (115 mg, 0.6 mmol) and HOBt hydrate (92 mg, 0.6 mmol) were added and the reaction mixture stirred at room temperature for 24 hrs. The solvent was evaporated in vacuo (45° C., 0.1 mbar) and the residue was triturated with DCM (10 mL) and filtered. The solid was triturated with hot acetonitrile, filtered hot and dried to afford 3-(aminosulfonyl)-N-[3-(2-quinoxalinyl)phenyl]propanamide (78 mg, 40%). LCMS calculated for C17H16N4O3S (M+H): 357.41. found 357.24. 1H-NMR (DMSO-d6, 400 Mhz) δH: 10.41 (1H, br.), 9.50 (1H, s), 8.53 (1H, m), 8.15 (2H, m), 8.02 (1H, m), 7.94-7.80 (3H, m), 7.55 (1H, m), 6.88 (2H, br.), 3.35 (2H, t, J=7.2 Hz), 2.85 (2H, t, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592415B2
Source datasetuspto-grants-2013_11
ORD IDord-75f1cf1e3555441a962ab91b71f5891c
Source noteuspto-grants-2013_11