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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872034Generated: October 27, 2026

Morpholine → tert-butyl cyclopropyl{[1-(3-methoxypropyl)-4-morpholin-4-yl-1H-indol-3-yl]methy}carbamate

https://huagongshe.com/reaction/872034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-indol-3-yl]methyl}cyclopropylcarbamateHCID 86645632—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Producttert-butyl cyclopropyl{[1-(3-methoxypropyl)-4-morpholin-4-yl-1H-indol-3-yl]methy}carbamateHCID 59494507—

Reaction Conditions

Temperature90 °C

Reaction Steps

Morpholine (73.5 μL), cetyltrimethylammoniumbromide (14.6 mg), bis(tri-tert-butylphosphine)palladium(0) (41 mg) and 50% aqueous solution of sodium hydroxide (96 μL) were added to a solution of tert-butyl {[4-bromo-1-(3-methoxypropyl)-1H-indol-3-yl]methy}cyclopropylcarbamate (205 mg) in toluene (3 ml) and the mixture was stirred under argon atmosphere at 90° C. for 23 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The obtained solution was 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 3/2) to give tert-butyl cyclopropyl{[1-(3-methoxypropyl)-4-morpholin-4-yl-1H-indol-3-yl]methy}carbamate (280 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-e9121c2e8655457db9f71a4596fe2744
Source noteuspto-grants-2015_03