HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631067Generated: October 25, 2026
Hydrochloric Acid → Ethyl 5-(4-Decanamidophenylsulfonamido)-1,3,4-thiadiazole-2-carboxylate
https://huagongshe.com/reaction/631067
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 5-amino-1,3,4-thiadiazole-2-carboxylate | HCID 2756556 | — |
| Reactant | 4-Decanamidobenzenesulfonyl chloride | HCID 86654301 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 5-(4-Decanamidophenylsulfonamido)-1,3,4-thiadiazole-2-carboxylate | HCID 53318403 | 65% |
Reaction Steps
To a solution of 4-decanamidobenzenesulfonyl chloride (220 mg, 0.64 mmol) in pyridine (4 mL) was added ethyl 5-amino-1,3,4-thiadiazole-2-carboxylate (100 mg, 0.58 mmol). The reaction mixture was stirred at room temperature for 4.5 h, then 2 M HCl (10 mL) was added to quench the reaction. The mixture was extracted with ethyl acetate (3×30 mL). The organic extracts were washed with water (20 mL), brine (20 mL), dried over Na2SO4, filtered, and concentrated. The residue was purified by chromatography on silica gel (70-230 mesh) eluted with CH2Cl2:methanol 9:1 to give the product as a solid, mp 101-102° C., in 65% yield (183 mg, 0.38 mmol); 1H NMR (300 MHz, DMSO-d6) δ 0.83 (t, 3H, J=6.6 Hz), 1.22-1.32 (m, 15H), 1.56 (m, 2H), 2.31 (t, 2H, J=6.0 Hz), 4.33 (q, 2H, J=7.6 Hz), 7.71 (m, 4H), 10.19 (s, 1H); 13C NMR (75 MHz, DMSO-d6) δ 14.6, 14.6, 22.8, 25.6, 29.3, 29.4, 29.5, 29.6, 31.3, 31.9, 37.1, 62.8, 119.1, 127.6, 136.8, 143.2, 147.7, 159.2, 170.3, 172.5; MS (LCQ, ESI+) Calcd for C21H31N4O5S2 483.2. found 483.1 (M+H)+. HRMS (ESI+, m/z) Calcd for C21H31N4O5S2 483.1736. found 483.1728 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320734B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-bb8ed0c77a034ecfbce6beb528f8e104 |
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| Source note | uspto-grants-2016_04 |
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