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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588985Generated: October 28, 2026

Cesium carbonate → HCID 86665191, compound

https://huagongshe.com/reaction/588985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
Reactant4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 12095870—
ReactantHCID 68749545HCID 68749545—
SolventDimethylformamideHCID 6228—
ProductHCID 86665191HCID 86665191—

Reaction Steps

To a solution of tert-butyl 5,6-bis(chloromethyl)pyridine-3-carboxylate (1.80 g, 6.52 mmol) in N,N-dimethylformamide (93.0 mL) was added 4-chloro-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (1.80 g, 10.62 mmol), cesium carbonate (3.65 g, 11.21 mmol), and sodium bromide (0.671 g, 6.52 mmol). After 30 min, saturated aqueous sodium bicarbonate was added and the mixture was washed with ethyl acetate (3×). The combined organics were washed with water (3×), brine (3×) and were dried with magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→10% methanol dichloromethane) then a second purification by silica gel chromatography (100% dichloromethane→30% ethyl acetate dichloromethane) gave the title compound as a racemic mixture. Chiral separation of the individual enantiomers was accomplished by use of HPLC using a 10 cm ChiralPak® AD column (60% EtOH hexanes with 0.1% diethylamine) to give the title compound as the 1st eluting enantiomer. MS: m/z=373.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227973B2
Source datasetuspto-grants-2016_01
ORD IDord-696b81b3b8254bcf81c2fe91915f8a28
Source noteuspto-grants-2016_01