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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872032Generated: October 30, 2026

Water → HCID 59494734, compound

https://huagongshe.com/reaction/872032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 86645633HCID 86645633—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59494734HCID 5949473498.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium carbonate (276 mg), phenylboronic acid (122 mg), dichlorobis(triphenylphosphine)palladium(II) (175 mg) and water (132 μl) were added to a solution of tert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-indazol-3-yl]methyl}cyclopropylcarbamate (218 mg) in 1,2-dichloroethane (11 ml) and the mixture was stirred under argon atmosphere at 80° C. for 1.5 hours. The reaction mixture was cooled to room temperature, poured into ice water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and saturated brine, 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=20/1 to 7/3) to give tert-butyl cyclopropyl{[1-(3-methoxypropyl)-4-phenyl-1H-indol-3-yl]methyl}carbamate (212 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-bd6bd410592d4d03bb771be72373f372
Source noteuspto-grants-2015_03