HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl 5-methyl-4-oxo-2-(thiophen-3-ylmethyl)-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Diethyl 5-amino-3-methylthiophene-2,4-dicarboxylate | HCID 78537 | — |
| Reactant | 3-Thienylacetonitrile | HCID 83730 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | Ethyl 5-methyl-4-oxo-2-(thiophen-3-ylmethyl)-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate | HCID 68664667 | — |
Reaction Steps
515 Milligrams of diethyl 5-amino-3-methylthiophene-2,4-dicarboxylate and 296 mg of 3-thiopheneacetonitrile were added to 8 mL of 4N hydrogen chloride-dioxane solution and stirred for 10 hours. Thereafter the liquid reaction mixture was poured on ice, and its pH was adjusted to 8-9 with 25% aqueous ammonia. Whereupon precipitated crystals were recovered by filtration and washed first with water, and then with hexane. The crude crystals were recrystallized from a liquid mixture of N,N-dimethylformamide and cyclohexane, to provide 397 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377944B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-c9af8f1317034c27b6e3a3a0c5a95503 |
| Source note | uspto-grants-2013_02 |