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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872039Generated: October 29, 2026

Water → HCID 59494651, compound

https://huagongshe.com/reaction/872039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl dihydrogen borateHCID 61925—
ReactantHCID 86645635HCID 86645635—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59494651HCID 5949465161.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

Potassium carbonate (207 mg), ethyl boric acid (92.4 mg) and bis(diphenylphosphino)ferrocene dichloropalladium(II) (36.6 mg) were added to a solution of tert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]methyl}cyclopropylcarbamate (219 mg) in 1,4-dioxane (14.5 ml) and the mixture was stirred under argon atmosphere at 110° C. for 3 hours. The reaction mixture was cooled to room temperature, water was added therein and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and saturated brine successively, dried over magnesium sulfate and concentrated in vacuo. The resulted residue was purified with a silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=4/1 to 1/3) to give tert-butyl cyclopropyl{[4-ethyl-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]methyl}carbamate (119 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-83ed266e488246d682c035e760e4718c
Source noteuspto-grants-2015_03