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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809697Generated: October 29, 2026

Sodium Bicarbonate → (6-Bromo-pyridin-2-yl)-(2,4-dichloro-pyrimidin-5-yl)-methanone

https://huagongshe.com/reaction/1809697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
Reactant(6-Bromo-pyridin-2-yl)-(2,4-dichloro-pyrimidin-5-yl)-methanolHCID 86667957—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(6-Bromo-pyridin-2-yl)-(2,4-dichloro-pyrimidin-5-yl)-methanoneHCID 86667958—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of crude (6-bromo-pyridin-2-yl)-(2,4-dichloro-pyrimidin-5-yl)-methanol (from Example 28 supra) (16.1 g, crude) in dichloromethane (200 mL), water (20 mL) was added followed by NaHCO3 (2.1 g, 25 mmol), TBAB (485 mg, 1.5 mmol) and TEMPO (90 mg, 0.5 mmol). The mixture was then cooled to 0° C. and NaClO (70 mL, active chloride >6.0%) was added slowly and the resulting mixture was stirred for 30 minutes. The mixture was poured into water and extracted with dichloromethane. The organic phase was dried over anhydrous MgSO4, filtered and concentrated. The residue was purified by column chromatography (silica gel, eluting with ethyl acetate:petroleum ether, 1:20) to give (6-bromo-pyridin-2-yl)-(2,4-dichloro-pyrimidin-5-yl)-methanone as a white solid. (Yield 12.7 g, 76% over two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362023B2
Source datasetuspto-grants-2013_01
ORD IDord-25de5dddf1f9471b9331a7acf7b73c12
Source noteuspto-grants-2013_01