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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024651Generated: October 29, 2026

Cesium carbonate → HCID 24781189, compound

https://huagongshe.com/reaction/1024651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant5-BromopyrimidineHCID 78344—
ReactantHCID 57899408HCID 57899408—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 24781189HCID 24781189—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 5-(4-chloro-phenyl)-1-(3-methanesulfonyl-phenyl)-6-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1,5-dihydro-pyrazolo[3,4-d]-pyrimidin-4-one (prepared as described in example 51, 0.500 g, 0.829 mmol) in N,N-dimethylformamide (20 mL) is degassed with argon for 0.5 h. Then 5-bromopyrimidine (0.200 g, 1.24 mmol), cesium carbonate (0.540 g, 1.66 mmol), Pd(dppf)2Cl2 (0.060 g, 0.082 mmol) is added and the resulted mixture is degassed with argon for 0.5 h. The reaction mixture is then heated at 100° C. for 2 h. The reaction mixture is cooled to rt and diluted with water and extracted with ethyl acetate (3×). The combined organic layer is washed with brine, dried over Na2SO4, concentrated, and purified by column chromatography over silica gel (60-120 mesh) to afford 5-(4-chloro-phenyl)-1-(3-methanesulfonyl-phenyl)-6-(4-pyrimidin-5-yl-phenyl)-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one. 1H NMR (DMSO-d6, 400 MHz) δ 9.18 (s, 1H), 9.15 (m, 2H), 8.67 (m, 1H), 8.61 (m, 1H), 8.55 (m, 1H), 7.96 (m, 1H), 7.90 (m, 1H), 7.82 (m, 2H), 7.61 (m, 2H), 7.46 (m, 4H), 3.30 (s, 3H); LC-MS calculated for C28H19ClN6O3S (M+H+) 555.1, found 554.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722691B2
Source datasetuspto-grants-2014_05
ORD IDord-eab0f52c87f74ac6a3fb5229771347f0
Source noteuspto-grants-2014_05