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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591343Generated: November 1, 2026

Triethylamine → di-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate

https://huagongshe.com/reaction/591343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
Reactantdi-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-hydroxyethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamateHCID 117812722—
SolventTetrahydrofuranHCID 8028—
Productdi-tert-butyl (4R)-N-(tert-butoxycarbonyl)-4-{[1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamateHCID 117812673—

Reaction Steps

Di-tert-butyl (4R)—N-(tert-butoxycarbonyl)-4-{[1-(2-hydroxyethyl)-1H-1,2,3-triazol-4-yl]methyl}-L-glutamate (74 mg, 152.7 μmol) was dissolved in tetrahydrofuran (5 ml) and triethyl amine (319 μl, 2.3 mmol), Nonafluorobutanesulfonyl fluoride (185 mg, 611 μmol), and Triethylamine trihydrofluoride (98 mg, 611 mmol) were added subsequently. The mixture was stirred at room temperature for 6 days. The mixture was than concentrated in vacuo, and the residue was purified by silica gel chromatography to yield 30 mg (40%) of slightly impure product, which was used in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-cd1141b71fa146afa79ebb0b93ce594e
Source noteuspto-grants-2016_01