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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394329Generated: October 30, 2026

Diethyl Malonate → 5-chloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/2394329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant3-Amino-6-bis(ethoxycarbonyl)methyl-2-chloropyridineHCID 10517360—
Reactant3-Amino-2-bis(ethoxycarbonyl)methyl-6-chloropyridineHCID 10589329—
SolventHydrochloric AcidHCID 313—
Product5-chloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-oneHCID 10654688—

Reaction Steps

The mixture containing 3-amino-2-bis(ethoxycarbonyl)methyl-6-chloropyridine, 3-amino-6-bis(ethoxycarbonyl)methyl-2-chloropyridine and diethyl malonate was taken up in 6N HCl solution (700 mL) and heated at reflux for 5 hours. After removing the aqueous acid in vacuo, the residue was taken up in water and again concentrated to yield 5-chloro-4-azaoxindole as a brown solid which was dried in the air. The yield was 7.04 g. (32% overall from 2,6-dichloro-3-nitropyridine). An analytical sample was prepared by recrystallization from isopropanol; m.p. 250°-254° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-040800c009b843f88f1782ad86d73ea9
Source noteuspto-grants-1998_09