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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072916Generated: October 30, 2026

Triethylamine → HCID 14390498, compound

https://huagongshe.com/reaction/2072916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Fluorobenzoyl chlorideHCID 74376—
ReactantEthyl 2-[(3-nitropyridin-2-YL)amino]acetateHCID 14062544—
ReactantEthyl 2-(3-aminopyridin-2-ylamino)acetateHCID 14390203—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390498HCID 143904986.6%

Reaction Steps

Under a nitrogen atmosphere, 3-fluorobenzoyl chloride (12.9 g, 0.0816 mole) was added dropwise to a stirred and chilled (10°-15° C.) mixture of N-(3-amino-2-pyridinyl)glycine ethyl ester (0.0816 mole) [freshly prepared by the hydrogenation of a solution of N-(3-nitro-2-pyridinyl)glycine ethyl ester in tetrahydrofuran over 5% palladium on carbon at room temperature], triethylamine (8.3 g, 0.0816 mole), anhydrous tetrahydrofuran (200 ml), and powdered molecular sieves. The reaction mixture was stirred at room temperature for 1 hour and was filtered. The filtrate was concentrated in vacuo and the residual solid triturated in isopropyl ether-isopropyl alcohol, giving 24.2 g (94%). Recrystallization of a 2.0-g sample gave 1.72 g of a white powder, mp 134°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-b6bb195fcf234cf3a52d0ab2e9483cca
Source noteuspto-grants-1990_04