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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721497Generated: October 30, 2026

Triphosgene → HCID 21891033, compound

https://huagongshe.com/reaction/721497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
Reactant4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitroanilineHCID 17755401—
Reactant1-(Cyclohexylmethyl)pyrrolidin-3-amineHCID 21890640—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 21891033HCID 2189103321.1%

Reaction Steps

Chloroform (13 ml) and triethylamine (2 ml) were added to 4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2-nitroaniline (100 mg) to prepare a solution. Triphosgene (96 mg) was added to the solution, and the mixture was stirred at room temperature for 30 min. 1-(Cyclohexylmethyl)-3-pyrrolidinamine (64 mg) was then added thereto, and the mixture was stirred at room temperature overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The extract was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography using chloroform/acetone for development. Diethyl ether was added to the purification product, and the precipitated crystal was collected by filtration and was washed to give the title compound (34 mg, yield 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-33677ad66ceb488aa947b1b1478898bc
Source noteuspto-grants-2006_11