Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | HCID 178527385 | HCID 178527385 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13536373 | HCID 13536373 | 98% |
Reaction Steps
Diethylcarbamoyl chloride (1.55 ml; 11.8 mmol) was added to cyclopropylmethyl 1,2,4-triazol-3-yl sulfone (2.07 g; 11.1 mmol) in dry pyridine (10 ml) under dry nitrogen. The resulting solution was stirred at room temperature overnight. The resulting mixture was poured into cold 2M hydrochloric acid (40 ml) and the cloudy solution extracted into ethyl acetate (3×50 ml). The extracts were combined, washed with saturated brine (50 ml), dried (Na2SO4), filtered and evaporated to afford 3-(cyclopropylmethylsulfonyl)-N,N-diethyl-1,2,4-triazole-1-carboxamide (3.10 g; 98%) as white crystals, m.p. 68°-74° C., (Found, C: 46.23; H: 6.24; N: 19.60; S: 11.29. C11H18N4O3S requires C: 46.14; H: 6.34; N: 19.57; S: 11.20%) NMR - d(CDC13; 60 MHz) 0.2-0.9 (4H, m), 0.9-1.5 (7H, m), 3.3 (2H, d, J= 7 Hz), 3.6 (4H, q, J=7 Hz) and 8.9 (1H, s). IR vmax (CHCl3) 3040, 1710, 1440, 1340, 1270, 1180, 1150, 1030, 870 and 635 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05308830 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-7fb9861988ef4a53b41a0f9a152cf12b |
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| Source note | uspto-grants-1994_05 |
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