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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348578Generated: November 3, 2026

Water → (1S)-5-(1-Methyl-6-oxo-4-pyridin-4-yl-1,6-dihydro-pyrimidin-2-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1348578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one hydrochlorideHCID 23024527—
Reactant(1S,4S)-(-)-2-Boc-2,5-diazabicyclo[2.2.1]heptaneHCID 66592084—
SolventDimethylformamideHCID 6228—
Product(1S)-5-(1-Methyl-6-oxo-4-pyridin-4-yl-1,6-dihydro-pyrimidin-2-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl esterHCID 6880188072.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture containing 10.7 ml (78.14 mmol) of triethylamine, 13.6 g (52.7 mmol) of 2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one hydrochloride (1:1), 6.0 g (30.24 mmol) of (1S)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester in 500 ml of anhydrous dimethylformamide is stirred at 20° C. for 6 h. Water is added to the cooled mixture and the resulting solution extracted with ethyl acetate. The combined extracts are washed with saturated aqueous ammonium chloride and saturated aqueous sodium chloride then-evaporated. The crude product is refluxed in diethylether for 1 h to afford 8.36 g of pure product as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211581B2
Source datasetuspto-grants-2007_05
ORD IDord-0c65aa05e37f49ecb6cd4748622a6d81
Source noteuspto-grants-2007_05