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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849217Generated: October 30, 2026

Phosphorus oxychloride → 1-(2-Methyl-4-benzyloxyphenyl)-4-[(2-hydroxyethyl)amino]-6-beta,beta,beta-trifluoroethoxy-2,3-dihydropyrrolo[3,2-c]quinoline

https://huagongshe.com/reaction/849217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-(2-Methyl-4-benzyloxyphenyl)-4-oxo-6-beta,beta,beta-trifluoroethoxy-2,3,4,5-tetrahydropyrrolo[3,2-c]quinolineHCID 19369761—
Product1-(2-Methyl-4-benzyloxyphenyl)-4-[(2-hydroxyethyl)amino]-6-beta,beta,beta-trifluoroethoxy-2,3-dihydropyrrolo[3,2-c]quinolineHCID 19369834116%

Reaction Conditions

Temperature110 °C

Reaction Steps

1-(2-Methyl-4-benzyloxyphenyl)-4-oxo-6-β,β,β-trifluoroethoxy-2,3,4,5-tetrahydropyrrolo[3,2-c]quinoline(2.7 g, 5.6 mmol) was mixed with phosphoryl chloride(15 ml), and stirred at 110° C. for 30 minutes. After removing the excess phosphoryl chloride by distillation, the residue was dissolved in dichloromethane (50 ml), neutralized with aqueous solution of sodium bicarbonate, and stirred at room temperature for 30 minutes. The reaction mixture was extracted with dichloromethane, and the organic layer was washed with water for 3 times. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography(ethyl acetate:hexane=1:10) to obtain 1.7 g of desired compound as solid in 60% of yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011044
Source datasetuspto-grants-2000_01
ORD IDord-06edcc5da3f54e1a9c9859d4ac184fac
Source noteuspto-grants-2000_01