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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189334Generated: October 30, 2026

Cesium carbonate → HCID 69079901, compound

https://huagongshe.com/reaction/2189334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactanttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 11737525—
Reactant2-chloro-7-cyclopentyl-5-methyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl esterHCID 86637352—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 69079901HCID 6907990117.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-7-cyclopentyl-5-methyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl ester (110 mg, 0.374 mmol), 4-(6-Amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (114.66 mg, 0.412 mmol), Pd2(dba)3 (17.144 mg, 0.02 mmol), Xantphos (21.67 mg, 0.037 mmol) and cesium carbonate (183 mg, 0.562 mmol) in dioxane (5 mL) is degassed and back-filled with nitrogen three times. The reaction mixture is heated to 100° C. for 4 h. Water is added and the solution is extracted with ethyl acetate three times. The organic layers are combined, washed with brine and dried over anhydrous sodium sulfate. The solvent is evaporated and the crude product is dissolved in a small amount of ethyl acetate. White solid precipitates out and filters to give 2-[5-(4-tert-Butoxycarbonyl-piperazin-1-yl)-pyridin-2-ylamino]-7-cyclopentyl-5-methyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl ester as a white solid (35 mg, 17%) which was carried onto the next step without further purification. [M+H]+=536.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324225B2
Source datasetuspto-grants-2012_12
ORD IDord-7ce60a41f2184673a30b1c2b3c9a3da6
Source noteuspto-grants-2012_12