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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271819Generated: November 2, 2026

Cesium carbonate → HCID 178519798, compound

https://huagongshe.com/reaction/2271819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 66715127—
ReactantHCID 178519792HCID 178519792—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178519798HCID 17851979841%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of (6-bromo-4-((trans-4-(pyrrolidin-1-ylmethyl)cyclohexyl)amino)quinolin-3-yl)(cyclopropyl)methanone (46 mg, 0.10 mmol), 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (43 mg, 0.15 mmol) and Pd(dppf)Cl2 (11 mg, 0.015 mmol) in dioxane (4 mL) was added Cs2CO3 (1.0 M in H2O, 0.4 mL, 0.4 mmol). N2 gas was bubbled through the reaction mixture and the mixture was then heated at 80° C. for 2 h. The solution was allowed to cool to room temperature, then directly subjected to column chromatography (silica, 0-20% methanol/dichloromethane). The resultant residue was dissolved in ethyl acetate and washed with saturated sodium bicarbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated to afford the desired product (22.1 mg, 41%) as a yellow solid. 1H NMR (500 MHz, MeOD) δ 9.09 (s, 1H), 8.28 (d, J=2.1 Hz, 1H), 7.97-7.91 (m, 1H), 7.84 (d, J=8.7 Hz, 1H), 7.55 (s, 2H), 4.19-4.10 (m, 1H), 3.14-3.07 (m, 4H), 2.89-2.78 (m, 3H), 2.31 (d, J=12.6 Hz, 5H), 2.04-1.97 (m, 4H), 1.83-1.79 (m, 1H), 1.57 (q, J=12.3 Hz, 4H), 1.32-1.04 (m, 6H). ESI MS m/z 538 [C30H33O2N3O2+H]+; HPLC>99% (AUC), tR=11.29 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-272fae7b52a84d128b6ca30ae9301ce4
Source noteuspto-grants-2015_09