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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392983Generated: November 1, 2026

4-Bromobenzophenone → HCID 10157263, compound

https://huagongshe.com/reaction/1392983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzophenoneHCID 7030—
ReactantCesium carbonateHCID 10796—
Reactant4-(Imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-amineHCID 69197864—
CatalystPalladiumHCID 23938—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 10157263HCID 1015726358%

Reaction Steps

The title compound was prepared from 2-amino-4-(imidazo-[1,2-a]pyridin-3-yl)pyrimidine and 4-bromobenzophenone following the general method of Example 1 using cesium carbonate as the base and tris(dibenzylideneacetone)dipalladium (0) as the palladium source. The crude product was purified by column chromatography on silica gel using chloroform/ethanol, 95:5, as the eluent affording 0.14 g (58% yield) of the title compound as a yellow solid: mp (decomp.) 249-255° C.; MS (TSP) m/z 392 (M+1 ), 1H NMR (400 MHz, DMSO-d6) δ 10.38 (s, 1 H), 10.35 (d, J=6.8 Hz, 1 H), 9.03 (s, 1 H), 8.67 (d, J=5.4 Hz, 1 H), 8.01 (d, J=8.7 Hz, 2 H), 7.98 (m, 1 H), 7.87 (m, 1 H), 7.83 (d, J=8.7 Hz, 2 H), 7.76 (d, J=7.0 Hz; 2 H), 7.69 (m, 1 H), 7.59 (m, 3 H), 7.47 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345050B2
Source datasetuspto-grants-2008_03
ORD IDord-39e481e6b4174de1b273f63094f8c727
Source noteuspto-grants-2008_03