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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53443Generated: October 25, 2026

Pyridine → 2-Valerylamino-5-bromo-4-methyl-3-nitropyridine

https://huagongshe.com/reaction/53443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantValeryl chlorideHCID 61186—
Reactant2-Amino-5-bromo-4-methyl-3-nitropyridineHCID 7213207—
SolventWaterHCID 962—
Product2-Valerylamino-5-bromo-4-methyl-3-nitropyridineHCID 2146417381%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture comprising 10 g (43.1 mmol) of 2-amino-5-bromo-4-methyl-3-nitropyridine and 6.8 g of pyridine was heated to 110° C. in a nitrogen atmosphere. 5.7 g (47.4 mmol) of valeroyl chloride was dropwise added thereto and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was brought to room temperature, followed by the addition of methylene chloride (50 ml) and water (50 ml). The organic phase was separated. The aqueous phase was further extracted with methylene chloride (50 ml). The organic phases were combined, dried over anhydrous magnesium sulfate and subjected to vacuum concentration to give a crude crystal. It was recrystallized from ethyl acetate to give 11 g of 2-valerylamino-5-bromo-4-methyl-3-nitropyridine (yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618969
Source datasetuspto-grants-1997_04
ORD IDord-1da1f522f51f4cdfa04c306c6fee3dc0
Source noteuspto-grants-1997_04