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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767063Generated: October 31, 2026

Water → HCID 24884767, compound

https://huagongshe.com/reaction/1767063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 24884768HCID 24884768—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 24884767HCID 2488476755.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

A solution of 0.22 g (0.52 mmol) of (+/−)9-(2-chloro-6,7-dihydro-5H-[1]pyrindin-6-ylmethyl)-7,7-dimethyl-2-(pyrimidin-4-yl)-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-one in 3 ml of anhydrous toluene and 0.5 ml of ethanol was treated with 0.625 ml (2M solution in water) of sodium carbonate, 36 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium and 0.095 g (0.780 mmol) of phenyl-boronic acid. After being stirred for 24 h at 140° C., water was added, the mixture was extracted with dichlomethane. The organic phase was dried and evaporated to give crude product, which was purified by silica gel chromatography, eluting with dichloromethane/methanol/ammonia in the proportions 99/1/0.1 to give 0.133 g of pure product obtained in the form of free base. Mp: 209–211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232827B2
Source datasetuspto-grants-2007_06
ORD IDord-df23ab4b31254e10ac8a449edecca02c
Source noteuspto-grants-2007_06