Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351826Generated: November 2, 2026

Triethylamine → HCID 54412940, compound

https://huagongshe.com/reaction/2351826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant4-AminopyrimidineHCID 68958—
ReactantHCID 53809092HCID 53809092—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54412940HCID 54412940136.8%

Reaction Steps

N-(t-butoxycarbonyl)-3-phenoxyphenylalanine (1 g) was dissolved in dry tetrahydrofuran (30 ml) and triethylamine (2 ml) was added thereto. Thereafter, ethyl chlorocarbonate (0.3 g) was added under ice-cooling, followed by stirring for 30 minutes. To this solution, 4-aminopyrimidine (0.24 g) was added, followed by stirring at room temperature for 10 hours. After distilling off the solvent, the residue was extracted with ethyl acetate, followed by washing with water. After drying, the solvent was distilled off to obtain N-(t-butoxycarbonyl)-3-phenoxy-DL-phenylalanine 4-pyrimidylamide (I) (1.5 g), which was confirmed as a substantially pure product by an NMR analysis, in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873253
Source datasetuspto-grants-1989_10
ORD IDord-fefeb7041c8b4d22bd3724cc901a4d72
Source noteuspto-grants-1989_10