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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666568Generated: October 31, 2026

1,2-Dichloroethane → HCID 24959464, compound

https://huagongshe.com/reaction/1666568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
ReactantHOAtHCID 181649—
Reactant2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazoleHCID 554208—
ReactantHCID 59591413HCID 59591413—
ProductHCID 24959464HCID 2495946419%

Reaction Steps

To a 20 ml scintillation vial was added EDC (54 mg, 0.283 mmol), HOAt (38 mg, 0.283 mmol) and commercially available 5-(4-fluorophenyl)-1,3,4-thiadiazol-2-amine (55 mg, 0.283 mmol). To this was added 5-[(ethylamino)sulfonyl]-2,3-difluorobenzoic acid as a solution in 2 ml DMF (75 mg, 0.283 mmol based on theoretical yield of preceding). The reaction mixture was stirred at room temperature overnight with a Teflon covered magnetic stir-bar. The reaction mixture was then concentrated to ˜1 ml and the residue was purified using a Gilson preparative HPLC system with a Waters Xterra (C-18) column 100 mm by 50 mm ID, eluting with 30% B to 60% B in 10 min, where A=H2O and B=CH3CN pumped at 150 mL/min to yield 5-[(Ethylamino)sulfonyl]-2,3-difluoro-N-[5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl]benzamide as a white solid (12 mg, 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044075B2
Source datasetuspto-grants-2011_10
ORD IDord-c6cbdb51e3f448508a96e425c9357db1
Source noteuspto-grants-2011_10