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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250606Generated: November 1, 2026

Allylamine → HCID 18326474, compound

https://huagongshe.com/reaction/1250606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN,N-bis(1-methylethyl)formamideHCID 75912—
Reactant6-Nitro-2,4(1H,3H)-quinazolinedioneHCID 816982—
SolventWaterHCID 962—
ProductHCID 18326474HCID 1832647412.6%

Reaction Steps

To 250 mg (1.21 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 5.00 ml (53.64 mmol) of phosphorus oxychloride and 0.18 ml (1.21 mmol) of diisopropylformamide, and the resulting mixture was subjected to heating under reflux for 24 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 5 ml of acetonitrile, followed by addition of 328 mg (2.42 mmol) of 2,2,2-trifluoroethylamine hydrochloride and 1.69 ml (12.10 mmol) of triethylamine under ice cooling and stirring under ice cooling for 30 minutes. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, 1.50 ml (20.00 mmol) of allylamine was added thereto, followed by stirring overnight, adding water to the reaction solution, extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 50 mg (12.6%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-00f941b5b9464fa1b079ca3fff9a2cfa
Source noteuspto-grants-2002_01