HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-1-propanol → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropyloxy)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-methylsulphonylpyrimidine | HCID 21279770 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropyloxy)pyrimidine | HCID 21298814 | 47.5% |
Reaction Steps
4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-methylsulphonylpyrimidine (0.15 g.) was added to a mixture of 3-aminopropanol (0.075 g.), t-butanol (5 ml.) and a 50% w/w dispersion of sodium hydride in mineral oil (0.05 g.) which was stirred under an argon atmosphere. The mixture was stirred at room temperature for 2 hours, heated under reflux for 4 hours and then evaporated to dryness. The residue was partitioned between 2N aqueous acetic acid and ether, and the aqueous phase basified with 17N NaOH and extracted three times with ether. The combined ether extracts were dried and evaporated to dryness to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-(3-aminopropyloxy)pyrimidine (0.07 g.) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762932 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-31ecbbacedb24809b4177087bbf70ce6 |
| Source note | uspto-grants-1988_08 |