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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844443Generated: October 30, 2026

Hydrochloric Acid → benzyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylate

https://huagongshe.com/reaction/844443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl N-(3-methylpyridin-4-yl)carbamateHCID 15273533—
ReactantBenzyloxalateHCID 19738602—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Productbenzyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylateHCID 2261256744.6%

Reaction Conditions

Temperature-40 °C

Reaction Steps

40 ml of 1.7M tert-butyllithium in pentane are added, at −40° C. under nitrogen, to 5 g of 4-(N-Bocamino)-3-methylpyridine. After stirring for 1 hour at −40° C., the lithiated derivative thus formed is added to 12.9 g of benzyl oxalate in 100 ml of THF at −40° C. The mixture is allowed to return to 0° C., it is left stirring for 2 hours, 25 ml of 6N HCl are then added and this mixture is heated at 50° C. for one and a half hours. The pH is brought to 9 by addition of 1N NaOH, the mixture is then extracted with EtOAc and the extracts are dried and evaporated. The residue is chromatographed on silica, eluting with DCM/MeOR (100/3; v/v) to give 2.7 g of the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380230B1
Source datasetuspto-grants-2002_04
ORD IDord-7407aa4c38a749dd8bf6c668938032d6
Source noteuspto-grants-2002_04