HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364265Generated: October 26, 2026
Ammonia → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidine
https://huagongshe.com/reaction/364265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-[3-(2,2,2-Trifluoroethyl)thioureido]-[(3-phthalimido)propylthio]pyrimidine | HCID 86738667 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropylthio)pyrimidine | HCID 21298711 | — |
Reaction Steps
A mixture of 4-[3-(2,2,2-trifluoroethyl)thioureido]-[(3-phthalimido)propylthio]pyrimidine (0.4 g.), N,N-dimethylformamide (5 ml.), saturated ethanolic ammonia (10 ml.) and yellow mercuric oxide (280 mg.) was stirred at room temperature for 3 hours and then filtered and the filtrate evaporated to dryness. A solution of the residue in ethanol (10 ml.) was treated with hydrazine hydrate (1 ml.), the mixture heated under reflux for 1 hour and then evaporated to dryness. The residue was stirred with 1N hydrochloric acid and then filtered and the filtrate basified with 17N NaOH. The mixture was extracted with ether and the combined ether extracts dried and evaporated to dryness to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[(3-amino)propylthio]pyrimidine which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04604465 |
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| Source dataset | uspto-grants-1986_08 |
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| ORD ID | ord-e226bd60a9b542d98b179fabf64af1a0 |
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| Source note | uspto-grants-1986_08 |
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