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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503354Generated: October 26, 2026

Pyridine → HCID 59129340, compound

https://huagongshe.com/reaction/503354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantButyryl chlorideHCID 8855—
Reactant2-((1-Methylcyclopropyl)ethynyl)-4-nitroanilineHCID 59129519—
SolventDichloromethaneHCID 6344—
ProductHCID 59129340HCID 5912934082%

Reaction Steps

To a solution of 2-((1-methylcyclopropyl)ethynyl)-4-nitroaniline (220 mg, 1.0 mmol) and pyridine (160 mg, 2.0 mol) in CH2Cl2 (20 mL) was added butyryl chloride (140 mg, 1.3 mmol) at 0° C. The mixture was warmed to room temperature and stirred for 3 h. The mixture was poured into ice-water. The organic layer was separated and the aqueous phase was extracted with CH2Cl2 (30 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure to obtain N-[2-(1-methyl-cyclopropyl-ethynyl)-4-nitro-phenyl]-butyramide (230 mg, 82%), which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-8689ece752064200ae17c3a2a4057707
Source noteuspto-grants-2010_08