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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275778Generated: October 31, 2026

Ethyl (chloroformyl)acetate → HCID 86717889, compound

https://huagongshe.com/reaction/2275778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (chloroformyl)acetateHCID 118030—
Reactant3-(2,6-Difluoro-benzyloxy)-pyridin-2-ylamineHCID 10263498—
SolventEthanolHCID 702—
ProductHCID 86717889HCID 86717889—

Reaction Steps

1.93 g of 3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine (Example 1A; 8.2 mmol, 1 equivalent) were initially charged in 50 ml of ethanol, and 8.2 g of ethyl 2-chloro-3-oxopropanoate (75% pure, crude product from Example 26A, 40.8 mmol, 5 equivalents) were added. The reaction mixture was heated at reflux overnight. The mixture was then concentrated under reduced pressure and the crude product obtained was chromatographed on 340 g of silica gel (Biotage Isolera) (mobile phase: cyclohexane:ethyl acetate gradient; Rf value of the product in cyclohexane:ethyl acetate 2:1=0.36). The product fractions were combined and concentrated and the residue obtained was triturated with diisopropyl ether. The solid was filtered off and dried under high vacuum. This gave 2.02 g of the title compound (71% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126998B2
Source datasetuspto-grants-2015_09
ORD IDord-05d6a94b510243a0a46172869e5964ac
Source noteuspto-grants-2015_09