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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47213Generated: October 26, 2026

3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- → Tert-butyl 3-amino-3-(4-trifluoromethyl-3-pyridinecarbonyloxyimino)propionate

https://huagongshe.com/reaction/47213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-HCID 2777549—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactanttert-butyl 2-(N'-hydroxycarbamimidoyl)acetateHCID 76589802—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-amino-3-(4-trifluoromethyl-3-pyridinecarbonyloxyimino)propionateHCID 5393129951.6%

Reaction Steps

30 g of 4-trifluoromethyl-3-pyridinecarboxylic acid is initially charged in 150 ml of dry THF and, a little at a time, admixed with 25.3 g of carbonyl-diimidazole. The mixture is stirred at room temperature for 30 min. 27.2 g of tert-butoxycarbonylacetamide oxime dissolved in 150 ml of THF are then added dropwise. The mixture is stirred overnight, the solvent is evaporated and the residue is taken up in ethyl acetate, washed three times with 1 M sulfuric acid and once with saturated sodium bicarbonate solution. Concentration of the ethyl acetate phase gives 28 g of the product as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699853B2
Source datasetuspto-grants-2004_03
ORD IDord-9015caa220024c63a392dc2d18aba4db
Source noteuspto-grants-2004_03