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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795973Generated: November 2, 2026

Trifluoroacetic acid → 5-chloro-2-methyl-3H,4H-pyrrolo[2,1-f][1,2,4]triazin-4-one

https://huagongshe.com/reaction/1795973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactantmethyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochlorideHCID 67017160—
SolventAcetonitrileHCID 6342—
Product5-chloro-2-methyl-3H,4H-pyrrolo[2,1-f][1,2,4]triazin-4-oneHCID 13575250480.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 1-amino-3-chloro-1H-pyrrole-2-carboxylic acid methyl ester, hydrochloride salt (11.0 g, 52.1 mmol) and trifluoroacetic acid (6.0 mL, 77.9 mmol) in acetonitrile (230 mL) was heated at 85° C. overnight. The reaction mixture was concentrated and treated with fresh acetonitrile (200 mL) and triethylamine (22.0 mL, 157.8 mmol). The reaction mixture was heated at 85° C. overnight and concentrated to small volume and diluted with water (100 mL). The mixture was then stirred at rt for 20 min. The precipitate was collected, washed with water and dried to give the title compound as a brown solid (7.67 g, 80%): 1H NMR (CD3OD): δ 7.28 (s, 1H), 6.42 (s, 1H), 2.20 (s, 3H); MS (ESI+) 184.02, 186.10 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030118B2
Source datasetuspto-grants-2006_04
ORD IDord-0688be2c467148fd9c9a5ff41e7986b5
Source noteuspto-grants-2006_04