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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661998Generated: October 30, 2026

Cesium carbonate → HCID 56925086, compound

https://huagongshe.com/reaction/661998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-methoxy-2,5-dihydro-1H-pyrrol-2-oneHCID 574769—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantHCID 66606710HCID 66606710—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 56925086HCID 5692508627%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(3-bromo-2-methylphenyl)-7-(2-hydroxypropan-2-yl)-9H-carbazole-1-carboxamide (Intermediate 81-25, 70 mg, 0.160 mmol), 4-methoxy-1H-pyrrol-2(5H)-one (362 mg, 3.20 mmol), cesium carbonate (78 mg, 0.24 mmol), tris(dibenzylideneacetone)dipalladium (14.7 mg, 0.016 mmol) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos, 27.8 mg, 0.048 mmol) in 1,4-dioxane (2 mL) was purged with nitrogen and heated via microwave irradiation in a sealed tube at 100° C. for 1 h. The mixture was diluted with DCM, washed with NaHCO3 (aq), dried and concentrated. The residue was purified by preparative HPLC, and the appropriate effluent fractions were treated with NaHCO3 (aq) and extracted with DCM. The combined organic phases were washed with water, dried and concentrated to provide as a white solid (20 mg, 27%). 1H NMR (400 MHz, methanol-d4) δ 7.91 (1H, d, J=7.70 Hz), 7.73 (1H, d, J=0.88 Hz), 7.39-7.46 (2H, m), 7.31-7.34 (1H, m), 7.09 (1H, dd, J=8.47, 1.65 Hz), 7.01 (1H, d, J=7.70 Hz), 6.98 (1H, d, J=8.36 Hz), 5.29 (1H, s), 4.37-4.49 (2H, m), 3.91 (3H, s), 1.90 (3H, s), 1.58 (3H, s), 1.57 (3H, s). Mass spectrum m/z 492.0 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-37cfaa20aba248d0bff3161745ca11a0
Source noteuspto-grants-2011_12