HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045942Generated: November 1, 2026
1,2-Dichloroethane → HCID 46916507, compound
https://huagongshe.com/reaction/2045942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 3-(2-Quinoxalinyl)aniline | HCID 807264 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 3-Sulfamoylpropanoic acid | HCID 21718767 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46916507 | HCID 46916507 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592415B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-75f1cf1e3555441a962ab91b71f5891c |
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| Source note | uspto-grants-2013_11 |
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