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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767562Generated: October 31, 2026

1-[3-(Benzyloxy)propyl]-3,3-dibromo-5-methoxy-1,3-dihydro-2H-pyrrolo[3,2-b]pyridin-2-one → 1-[3-(Benzyloxy)propyl]-5-methoxy-1,3-dihydro-2h-pyrrolo[3,2-b]pyridin-2-one

https://huagongshe.com/reaction/1767562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3-(Benzyloxy)propyl]-3,3-dibromo-5-methoxy-1,3-dihydro-2H-pyrrolo[3,2-b]pyridin-2-oneHCID 11328879—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product1-[3-(Benzyloxy)propyl]-5-methoxy-1,3-dihydro-2h-pyrrolo[3,2-b]pyridin-2-oneHCID 12035123—

Reaction Steps

Under argon and at room temperature, 1.10 g (16.8 mmol) of powdered zinc are added in portions to 789 mg (1.68 mmol) of the compound obtained in Step B dissolved in 15 ml of acetic acid. After 5 hours' stirring at room temperature, the reaction mixture is filtered using a Büchner funnel, evaporated to dryness and then coevaporated in the presence of toluene. The residue, which is taken up in ethyl acetate, is washed several times with water. The organic phase is dried over magnesium sulphate, filtered and concentrated and then purified by flash chromatography over silica gel (eluant:petroleum ether/ethyl acetate, 1:1) to yield the title compound in the form of an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235550B2
Source datasetuspto-grants-2007_06
ORD IDord-f8805e4e3c85466d8c22e40477d6389a
Source noteuspto-grants-2007_06