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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819488Generated: October 30, 2026

Sulfuric Acid → N-(5-chloro-2-oxo-1,2-dihydro-pyridin-4-ylmethyl)-acetamide

https://huagongshe.com/reaction/1819488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
ReactantN-(2,5-Dichloro-pyridin-4-ylmethyl)-acetamideHCID 57885548—
SolventWaterHCID 962—
ProductN-(5-chloro-2-oxo-1,2-dihydro-pyridin-4-ylmethyl)-acetamideHCID 69063784—

Reaction Conditions

Temperature200 °C

Reaction Steps

Compound N-(2,5-dichloro-pyridin-4-ylmethyl)-acetamide (250 mg, 1.14 mmol) was added to 33% H2SO4 (3 mL) and the mixture heated in a CEM microwave reactor at 200° C. for 30 min. After cooling to room temperature, the reaction mixture was diluted with water (20 mL) and basified with excess concentrated NH4OH. The reaction mixture was then frozen using a dry ice/acetone bath and evaporated to dryness in vacuo overnight in a freeze-dry apparatus. The solids were purified by column chromatography using a 12 g ISCO combi-flash column and dry-loading cartridge (silica gel, 100:0 to 50:50 DCM:DCM/MeOH/NH4OH 6:3:1) to afford N-(5-chloro-2-oxo-1,2-dihydro-pyridin-4-ylmethyl)-acetamide (246 mg, quant.) as an off-white solid. This material was directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601714B2
Source datasetuspto-grants-2009_10
ORD IDord-e702dc0a00524a38aacd5d8567ac6a17
Source noteuspto-grants-2009_10