HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-(2,6-Dimethylphenyl)-2-ethylsulfanyl-3,5-dihydro-imidazol-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 2-[3-(2,6-Dimethylphenyl)-thioureido]-acetamide | HCID 53947974 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2,6-Dimethylphenyl)-2-ethylsulfanyl-3,5-dihydro-imidazol-4-one | HCID 44295503 | 28.7% |
Reaction Steps
The title compound was prepared by the procedure described in Example 12 using 8.0 g of 2-[3-(2,6-dimethylphenyl)-thioureido]-acetamide, 25.0 g of ethyl iodide, and (200 mL) ethanol. Crystallization from hexane/diethyl ether mixture afforded the title compound as a light yellow solid (2.4 g), m.p. 86°-88° C. Anal. Calcd. for. C12H16N2O S: C, 62.87; H, 6.49; N, 11.28. Found: C, 62.98; H, 6.57; N, 11.30. Mass spectrum (El, M.+) m/z 248 1H-NMR (DMSO-d6 ; 400 MHz) δ7.27-7.30 (m, 1H), 7.21 (m, 1H), 7.19 (m, 1H), 7.33 (d, 1H), 4.42 (s, 2H), 3.06 (q, 2H), 2.07 (s, 6H), and 1.26 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599829 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-169f5b9a0fab4c7a91ad4a8b4451f09a |
| Source note | uspto-grants-1997_02 |