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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250601Generated: October 27, 2026

Tert-Butylamine → 4-t-Butylamino-2-chloro-6-nitroquinazoline

https://huagongshe.com/reaction/1250601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN,N-bis(1-methylethyl)formamideHCID 75912—
Reactant6-Nitro-2,4(1H,3H)-quinazolinedioneHCID 816982—
SolventWaterHCID 962—
Product4-t-Butylamino-2-chloro-6-nitroquinazolineHCID 1832650664.2%

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 1.26 ml (12.10 mmol) of t-butylamine 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, the residue was purified by a silica gel column to give 218 mg (64.2%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-27d5da839434492eacac3aa1683bc395
Source noteuspto-grants-2002_01