Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | HCID 178527389 | HCID 178527389 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19026924 | HCID 19026924 | 98.7% |
Reaction Steps
Diethylcarbamoyl chloride (1.2 ml; 9.4 mmol) was added to cyclohexylmethyl 1,2,4-triazol-3-yl sulfone (2.0 g; 8.7 mmol) in dry pyridine (10 ml) under dry nitrogen, and the solution stirred at room temperature overnight. The resulting mixture was poured into 2M hydrochloric acid (40 ml) at 2° C. and the cloudy solution extracted into ethyl acetate (3×60 ml). The extracts were combined, dried (Na2SO4), filtered and evaporated, to afford a colorless oil which was dissolved in 95% dichloromethane, 5% acetonitrile, and the solution filtered through silica. Evaporation afforded 3-(cyclohexylmethylsulfonyl)-N,N-diethyl-1,2,4-triazole-1-carboxamide (2.82 g; 98%) as white crystals, m.p. 40°-46° C. (Found, C: 51.04; H: 7.39; N: 17.01; S: 9.81. C14H24N4O3S requires C: 51.20; H: 7.37; N: 17.06; S: 9.76%). NMR - d(CDCl3 ; 90 MHz) 0.80-2.30 (17H, m), 3.31 (2H, d, J=6.1 Hz), 3.61 (4H, m) and 8.92 (1H, s).
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-d2ed68abf89e4ca0bb0e96e2457ff1c4 |
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| Source note | uspto-grants-1994_05 |
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