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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978086Generated: October 31, 2026

Triethylamine → HCID 86756752, compound

https://huagongshe.com/reaction/1978086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantHCID 86756753HCID 86756753—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86756752HCID 8675675299.9%

Reaction Steps

A solution of 1.5 g of 2(R)-[1(S)-(tertbutoxycarbonyl)-4-methyl-3-pentenyl]-2′-isobutyl-2′-(methanesulphonyl)-4-methylvalerohydrazide, 0.51 g of triethylamine and 0.93 g trimethylsilyl triflate in 20 ml of 1,4-dioxane was heated at reflux under a nitrogen atmosphere for 4 hours. The mixture was cooled and the solvent was evaporated. The residue was dissolved in ethyl acetate and washed with 2M aqueous hydrochloric acid, water and brine. The ethyl acetate phase was then dried over anhydrous magnesium sulphate and the solvent was evaporated to give 1.31 g of 2(R)-[1(S)-(carboxy)-4-methyl-3-pentenyl]-2′-isobutyl-2′-(methanesulphonyl)-4-methylvalerohydrazide in the form of a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235787B1
Source datasetuspto-grants-2001_05
ORD IDord-73eb57dd8b2d4657b70ac4dabc2d0795
Source noteuspto-grants-2001_05