HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → HCID 20208695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidine | HCID 21298711 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20208695 | HCID 20208695 | — |
Reaction Steps
A mixture of 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidine (0.3 g.), ethyl formate (5 ml) and EtOH (2 ml.) was heated under reflux for 48 hours, then evaporated to dryness. The residue was dissolved in N aqueous HCl and the solution washed with EtOAc. The aqueous phase as basified with 10 N aqueous NaOH, extracted with EtOAc and the extract dried and evaporated to dryness. The residue was recrystallised from EtOAc to give N-[3-(4-[2-(2,2,2-trifluoroethyl)guanidino]pyrimid-2-ylthio)propyl]-formamide (0.2 g.), m.p. 165°-166°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496571 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-d0dda318e0c7489fa7bb60cd2782c00c |
| Source note | uspto-grants-1985_01 |