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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364290Generated: October 31, 2026

3-Amino-1-propanol → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropyloxy)pyrimidine

https://huagongshe.com/reaction/364290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-1-propanolHCID 9086—
ReactantSodium hydrideHCID 24758—
Reactant4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-methylsulphonylpyrimidineHCID 21279770—
Solventtert-ButanolHCID 6386—
Product4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(3-aminopropyloxy)pyrimidineHCID 2129881447.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604465
Source datasetuspto-grants-1986_08
ORD IDord-646353476b0143f19f831ad8ccb883e8
Source noteuspto-grants-1986_08