HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(Indan-5-yl)-1-isopropyl-2-thioxo-imidazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | NoName_76 | HCID 414244 | — |
| Reactant | 5-isothiocyanato-2,3-dihydro-1H-indene | HCID 2759357 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(Indan-5-yl)-1-isopropyl-2-thioxo-imidazolidin-4-one | HCID 15389491 | 36.1% |
Reaction Steps
The title compound was prepared by the procedure described in Example 18 using 17.5 g of indan-5-yl-isothiocyanate, 21.2 g of N-isopropyl glycine, 21.0 g of triethyl amine, and 300 mL of chloroform. Crystallization from ethanol afforded the title compound (9.9 g) as a white solid, m.p. 178°-180° C. Anal. Calcd. for. C15H18N2OS: C, 56.66; H, 6.61; N, 10.21. Found: C, 56.70; H, 6.67; N, 10.22. Mass spectrum (EI, M.+) m/z 274.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861517 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-bbdf46dbe9fe4895bc580feea3cdef89 |
| Source note | uspto-grants-1999_01 |