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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703288Generated: November 1, 2026

Hydrochloric Acid → Ethyl 1-(2-pyridylmethyl)-5-(4-phenylbenzoyl)pyrrole-3-carboxylate

https://huagongshe.com/reaction/1703288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl propiolateHCID 12182—
Reactant2-(4-Phenylbenzoylmethyl)imidazo [3,4-a]pyridinium BromideHCID 12897110—
ProductEthyl 1-(2-pyridylmethyl)-5-(4-phenylbenzoyl)pyrrole-3-carboxylateHCID 2040101332.3%

Reaction Steps

2-(4-Phenylbenzoylmethyl)imidazo[3,4-a]pyridinium bromide (16 g., 40 mmoles), potassium carbonate (22 g., 160 mmoles) and ethyl propiolate (6.4 ml., 48 mmoles) were combined according to the procedure of Example 69, stirred for approximately 16 hours at room temperature, then isolated and converted to hydrochloride according to the procedure of Example 69, to yield ethyl 1-(2-pyridylmethyl)-5-(4-phenylbenzoyl)pyrrole-3-carboxylate (5.3 g., intermediate Rf on silica gel thin layer chromatography with ethyl acetate/5% acetic acid as eluant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351843
Source datasetuspto-grants-1982_09
ORD IDord-476c4a242ce04f5f921a438f536478e0
Source noteuspto-grants-1982_09