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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271309Generated: October 26, 2026

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

https://huagongshe.com/reaction/271309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-3-methyl-6-(pyrimidin-4-YL)pyrimidin-4-oneHCID 17954460—
Reactant(1S,4S)-(-)-2-Boc-2,5-diazabicyclo[2.2.1]heptaneHCID 66592084—
SolventTetrahydrofuranHCID 8028—
Product(1S)-5-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yl)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl esterHCID 6691566999.3%

Reaction Steps

A mixture containing 1.95 ml (14 mmol) of triethylamine, 2.45 g (11 mmol) of 2-chloro-1-methyl-1H-[4,4′]bipyrimidinyl-6-one, 2.58 g (13 mmol) of (1S)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester in 100 ml of anhydrous tetrahydrofuran was stirred at room temperature for 2 h. Water was added to the cooled mixture and the resulting solution extracted with ethyl acetate. The combined extracts were washed with saturated aqueous ammonium chloride and evaporated. The crude product was purified by chromatography on silica gel eluting with a mixture of dichloromethane/methanol in the proportions 100/0 to 98/2 to afford 4.2 g of pure product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452897B2
Source datasetuspto-grants-2008_11
ORD IDord-c7c9edeb2ca4450ba0800d17cb2b1925
Source noteuspto-grants-2008_11