HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-(2-Chloro-6-methylphenyl)-2-ethylsulfanyl-3,5-dihydroimidazol-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 2-[3-(2-Chloro-6-methylphenyl)-thioureido]-acetamide | HCID 54394060 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-(2-Chloro-6-methylphenyl)-2-ethylsulfanyl-3,5-dihydroimidazol-4-one | HCID 44295822 | 36.4% |
Reaction Steps
The title compound was prepared by the procedure described in Example 6 using 12.9 g of 2-[3-(2-chloro-6-methylphenyl)-thioureido]-acetamide, and 18.0 g of ethyl iodide. The hydrochloride salt was prepared in ethereal hydrogen chloride. Crystallization from ethyl acetate afforded the title compound as the monohydrochloride as a light yellow solid (4.9 g), m.p. 152°-154° C. (dec.). Anal. Calcd. for. C12H13Cl N2O S. HCl: C, 47.22; H, 4.62; N, 9.18. Found: C, 46.99; H, 4.60; N, 9.16. Mass spectrum (+FAB, [M+H]+) m/z 269/271 1H-NMR (DMSO-d6 ; 400 MHz) δ8.28 (broad s, 2H), 7.51 (m, 1H), 7.44 (t, 1H), 7.39 (m, 1H), 4.51 (q, 2H), 3.12 (q, 2H), 2.17 (s, 3H), and 1.27 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599829 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-2e1bc665b30c43c794f116b1abffcea3 |
| Source note | uspto-grants-1997_02 |