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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241579Generated: October 30, 2026

4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazoline → HCID 10229547, compound

https://huagongshe.com/reaction/1241579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 11002191—
Reactant5-Bromo-2H-1,3-benzodioxol-4-amineHCID 21936013—
ReactantSodium hexamethyidisilazaneHCID 45051731—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 10229547HCID 1022954729.3%

Reaction Steps

Sodium hexamethyldisilazane (1M solution in THF; 0.626 ml) was added to a solution of 6-bromo-2,3-methylenedioxyaniline (0.135 g) in DMF (2 ml) and the mixture was stirred at ambient temperature for 30 minutes. A solution of 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (0.1 g) in DMF (3.5 ml) was added and the resultant mixture was stirred at ambient temperature for 3 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (2×). The organic phase was washed with water and with brine, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using an 80:17:3 mixture of methylene chloride, methanol and a saturated methanolic ammonia solution as eluent. There was thus obtained the title compound as a solid (0.045 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.4 (m, 1H), 1.7 (m, 3H), 1.85 (m, 2H), 2.3 (m, 2H), 2.95 (m, 2H), 3.25 (m, 2H), 3.55 (m, 2H), 4.05 (s, 3H), 4.3 (m, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.3 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M+H+ 515 and 517; Elemental Analysis: Found C, 55.74; H, 5.30; N, 10.76. C24H27BrN4O4 requires C, 55.93; H, 5.28; N, 10.87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115615B2
Source datasetuspto-grants-2006_10
ORD IDord-bcd3a672062c4b1bba6be9d012aed963
Source noteuspto-grants-2006_10