HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666568Generated: October 31, 2026
1,2-Dichloroethane → HCID 24959464, compound
https://huagongshe.com/reaction/1666568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazole | HCID 554208 | — |
| Reactant | HCID 59591413 | HCID 59591413 | — |
| Product | HCID 24959464 | HCID 24959464 | 19% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044075B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c6cbdb51e3f448508a96e425c9357db1 |
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| Source note | uspto-grants-2011_10 |
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