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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918013Generated: October 31, 2026

Cesium carbonate → 3-(6,7-Bis(2-methoxyethoxy)quinazolin-4-ylthio)aniline

https://huagongshe.com/reaction/1918013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-AminothiophenolHCID 31577—
Reactant4-Chloro-6,7-bis(2-methoxyethoxy)quinazolineHCID 11289942—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product3-(6,7-Bis(2-methoxyethoxy)quinazolin-4-ylthio)anilineHCID 6687687477.5%

Reaction Steps

3-Aminothiophenol (56 mg, 0.45 mmol) was treated with cesium carbonate (193 g, 0.59 mmol) in anhydrous tetrahydrofuran (22 mL) and the mixture stirred at room temperature for 30 minutes. 4-chloro-6,7-bis(2-methoxyethoxy)quinazoline (142 mg, 0.45 mmol) from Example 12A was added and the mixture stirred at 60° C. overnight. After cooling to room temperature the mixture was diluted with chloroform, water and brine were added and the organic phase separated. The water phase was extracted three times with chloroform, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane/methanol 9:1) to afford 3-(6,7-bis(2-methoxyethoxy)quinazolin-4-ylthio)aniline (140 mg, 77%) as a solid. 1H NMR (300 MHz, CDCl3) δ 8.75 (s, 1H), 7.41 (s, 1H), 7:26 (t, 2H), 6.99-6.94 (m, 2H), 6.74 (d, 1H), 4.30 (s, 4H), 3.99 (bs, 6H), 3.87 (s, 6H); LC-MS (ESI) m/z 402 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-7c994ce37b2a4bc8add8a9ba55c75464
Source noteuspto-grants-2013_12