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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19471Generated: October 30, 2026

Cesium carbonate → [4-(4-Imidazo[1,2-alpha]pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-morpholin-4-yl-methanone

https://huagongshe.com/reaction/19471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-[(4-Iodophenyl)carbonyl]morpholineHCID 772634—
Reactant4-(Imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-amineHCID 69197864—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product[4-(4-Imidazo[1,2-alpha]pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-morpholin-4-yl-methanoneHCID 16667321—

Reaction Steps

4-Imidazo[1,2-α]pyridin-3-yl-pyrimidin-2-ylamine(Bioorganic & Medicinal Chemistry Letters 2004, 14(9), 2245-2248) (0.20 g, 0.95 mmol), palladium acetate (9 mg, 0.038 mmol), Xanthphos (33 mg, 0.057 mmol), caesium carbonate (0.46 g, 1.4 mmol) and (4-iodo-phenyl)-morpholin-4-yl-methanone (Method 16a in WO 05/044814) (330 mg, 1.05 mmol) were added to dioxane (7 ml) under a inert atmosphere and heated at reflux for 6 hours. Purification on silica using 0-10% MeOH in DCM as eluent gave the title compound as a colourless foam. Further purification was achieved using RPHPLC to give a colourless foam (239 mg, 63%); 1H NMR (400.132 MHz) 10.13 (d, 1H), 9.89 (s, 1H), 8.64 (s, 1H), 8.48 (d, 1H), 7.85 (d, 2H), 7.79 (d, 1H), 7.52 (t, 1H), 7.46 (d, 1H), 7.43 (d, 2H), 7.16 (t, 1H), 3.65-3.60 (m, 4H), 3.58-3.51 (m, 4H); MH+ 401.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745428B2
Source datasetuspto-grants-2010_06
ORD IDord-bb8afc7a752247e9bfa7916dce534294
Source noteuspto-grants-2010_06