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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347517Generated: October 31, 2026

(3-Fluoro-4-(5-methyl-6-(2-morpholinoethoxy)pyrrolo[2,1-f][1,2,4]triazin-4-yloxy)phenyl)-N3-(4-fluorophenyl)malonamide, hydrochloride salt → 5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-one

https://huagongshe.com/reaction/347517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Fluoro-4-(5-methyl-6-(2-morpholinoethoxy)pyrrolo[2,1-f][1,2,4]triazin-4-yloxy)phenyl)-N3-(4-fluorophenyl)malonamide, hydrochloride saltHCID 131726240—
SolventFormamideHCID 713—
Product5-Chloropyrrolo[2,1-f][1,2,4]triazin-4(1H)-oneHCID 13574208667.2%

Reaction Steps

A solution of methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate (10.0 g, 57.3 mmol, WO 03/099286: Compound A of Example 9) in formamide (40 mL) was heated at 170° C. for 1 h and then at 190° C. for 1 h. Upon cooling to room temperature, the mixture solidified. The product was purified by recrystallization from ethyl acetate to give the title compound (6.53 g, 67%) as a white solid. 1H NMR (CDCl3) δ 10.24 (br s, 1H), 7.48 (d, 1H, J=3.6 Hz), 7.29 (d, 1H, J=2.8 Hz), 6.47 (d, 1H, J=2.8 Hz); MS(ESI+) m/z 170.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173031B2
Source datasetuspto-grants-2007_02
ORD IDord-86ab28101f004e829f685da9731a2551
Source noteuspto-grants-2007_02