HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5,5-Dimethyl-1-(2-(4-(5-tosylthiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazol-idine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Aminoethyl)-5,5-dimethylimidazolidine-2,4-dione | HCID 57428804 | — |
| Reactant | 2-Chloro-4-(5-tosylthiophen-2-yl)pyrimidine | HCID 60204428 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5,5-Dimethyl-1-(2-(4-(5-tosylthiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazol-idine-2,4-dione | HCID 60204427 | 50.1% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
A mixture of 2-chloro-4-(5-tosylthiophen-2-yl)pyrimidine (100 mg, 0.23 mmol), 1-(2-aminoethyl)-5,5-dimethylimidazolidine-2,4-dione (33 mg, 0.26 mmol) and triethylamine (28 mg, 0.27 mmol) in toluene (3 mL) was heated at 160° C. for 35 min in a Personal Chemistry microwave reactor. Upon cooling to rt the precipitate was filtered and washed with diethyl ether. The solid was put into 2 mL of methanol and the suspension was stirred for about 15 min and filtered to afford the title compound as pale yellow crystals (56 mg, 50%). MS (M+H)+ 486.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858785B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-fd668e436ffe483d8f224dd6387daa70 |
| Source note | uspto-grants-2010_12 |