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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872033Generated: October 25, 2026

Potassium Phosphate, Tribasic → tert-butyl {[4-benzyl-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamate

https://huagongshe.com/reaction/872033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-Benzyl-9-borabicyclo(3.3.1)nonaneHCID 4150924—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactanttert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamateHCID 86645632—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-butyl {[4-benzyl-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamateHCID 59494459499.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium phosphate (498 mg), a 0.5M tetrahydrofuran-solution of B-benzyl-9-BBN (2.8 ml), palladium acetate(II) (21 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (38.5 mg) were added to a solution of tert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamate (205 mg) in N,N-dimethylformamide (4.3 ml) and the mixture was stirred under argon atmosphere at 80° C. for 3 hours. The reaction mixture was diluted with ethyl acetate, washed with water 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=20/1 to 2/1) to give tert-butyl {[4-benzyl-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamate (210 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-1caa458c96fe4315a8c0783c0fc49078
Source noteuspto-grants-2015_03