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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414742Generated: October 31, 2026

HCID 21956178, compound → 6-Chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one

https://huagongshe.com/reaction/2414742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21956178HCID 21956178—
ReactantHCID 21956193HCID 21956193—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product6-Chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-oneHCID 21907047—

Reaction Steps

A solution of 2.36 g (7.26 mmol) of the mixture of 3,3-dibromo-6-chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one and 3,3,5-tribromo-6-chloro-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one in THF (70 mL) and saturated ammonium chloride solution (70 mL) was treated with, 6 g (92 mmol) of powdered zinc. The mixture was stirred for 2 h, and another 6 g (92 mmol) portion of zinc was added. Stirring was continued another 2 h. The zinc was filtered off and washed with ether. The ether phase was separated, and the aqueous phase was extracted twice with a 1:1 mixture of THF/ether. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. The crude residue was loaded onto 7.5 g of silica gel and chromatographed on silica gel, eluting with a 90% hexane/10% ethyl acetate to 66% hexane/33% ethyl acetate gradient to give 0.647 g of the title compound. 1H NMR (DMSO-d6): δ 3.57 (s, 2H), 7.04 (d, J=7.6 Hz, 1H), 7.61 (d, J=7.6 Hz, 1H), 11.2 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815439B2
Source datasetuspto-grants-2004_11
ORD IDord-6ac042b3acf54c5d94683b0c19ec4c77
Source noteuspto-grants-2004_11