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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984852Generated: October 30, 2026

Phosphorus oxychloride → Ethyl 4-chloro-5-methylpyrrolo[2,1-f][1,2,4]triazine-6-carboxylate

https://huagongshe.com/reaction/984852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178469453HCID 178469453—
SolventTolueneHCID 1140—
ProductEthyl 4-chloro-5-methylpyrrolo[2,1-f][1,2,4]triazine-6-carboxylateHCID 1799871999.7%

Reaction Steps

A mixture of 4-hydroxy-5-methylpyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acid ethyl ester (60.0 g, 271.2 mmol, for preparation see WO 0071129), phosphorus oxychloride (30.3 mL, 325.4 mmol) and diisopropylethyl amine (37.7 mL, 217 mmol) in toluene (800 mL) was heated to reflux under argon for 18 h and then cooled to room temperature. The mixture was concentrated on rotovap and the residue was diluted with dichloromethane (1000 mL) and cold sodium bicarbonate solution (300 mL). The resulting mixture was stirred at room temperature for 10 min. The separated organic layer was washed with cold brine (300 mL), dried, and concentrated in vacuo. The crude material was purified by chromatography on silica gel eluting with dichloromethane to provide the desired compound (64.8 g, 99%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869952B2
Source datasetuspto-grants-2005_03
ORD IDord-33f8b9e32eed4d1290fb0571958d8aa7
Source noteuspto-grants-2005_03