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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953473Generated: November 1, 2026

1-Bromo-3-chloropropane → HCID 15481567, compound

https://huagongshe.com/reaction/1953473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantCarbonate IonHCID 19660—
ReactantPotassiumHCID 5462222—
ReactantHCID 135484041HCID 135484041—
SolventDimethylformamideHCID 6228—
ProductHCID 15481567HCID 1548156747.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-methoxy-3-{2-[3-(2-quinolylmethoxy)benzyl]tetrazolyl}quinolin-2-one (1.00 g, 2.04 mmol), potassium, carbonate (564 mg, 4.08 mmol), 1-bromo-3-chloropropane (962 mg, 6.12 mmol), and DMF (100 ml) was stirred for four hours at a bath temperature of 60° C. The solvent of the reaction mixture was removed under reduced pressure. Water was then added to the mixture, and the mixture was extracted with chloroform-methanol (10:1). The thus-obtained organic phase was dried over magnesium sulfate anhydrate, and the solvent was removed under reduced pressure. The organic phase was then subjected to silica gel column chromatography (developer: chloroform-methanol (100:1)), purified, and crystallized from a chloroform-diethylether mixture, to thereby obtain the title compound (546 mg, 0.963 mmol, 47.2%) as pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117886
Source datasetuspto-grants-2000_09
ORD IDord-cdb19f67ebd0431da58c7ee6b7014985
Source noteuspto-grants-2000_09