HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-[2-(2,2,2-Trifluoroethyl)-guanidino]-2-[(2-phthalimidoethyl)thiomethyl]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-[3-(2,2,2-Trifluoroethyl)thioureido]-2-[(2-phthalimidoethyl)thiomethyl]pyrimidine | HCID 53848275 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(2,2,2-Trifluoroethyl)-guanidino]-2-[(2-phthalimidoethyl)thiomethyl]pyrimidine | HCID 21298750 | — |
Reaction Steps
A mixture of 4-[3-(2,2,2-trifluoroethyl)-thioureido]-2-[(2-phthalimidoethyl)thiomethyl]pyrimidine (6.8 g.), dimethylformamide (30 ml.), saturated ethanolic ammonia (5 ml.) and yellow mercuric oxide (6.5 g.) was stirred at room temperature for 2 hours and then filtered. The filtrate was evaporated to dryness and the residue triturated with ether and filtered to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[(2-phthalimidoethyl)thiomethyl]pyrimidine (5.6 g.), m.p. 167°-168° after crystallisation from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04362728 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-cb33b673e4334f67bcb0fb20fbf8c295 |
| Source note | uspto-grants-1982_12 |