Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132822Generated: October 30, 2026

Potassium Carbonate → {5-[3-(2-Aza-bicyclo[3.1.0]hex-2-yl)-propoxy]-1H-indol-2-yl}-morpholin-4-yl-methanone

https://huagongshe.com/reaction/132822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Azabicyclo[3.1.0]hexane hydrochlorideHCID 67358156—
Reactant[5-(3-Chloro-propoxy)-1H-indol-2-yl]-morpholin-4-yl-methanoneHCID 67527317—
SolventAcetonitrileHCID 6342—
Product{5-[3-(2-Aza-bicyclo[3.1.0]hex-2-yl)-propoxy]-1H-indol-2-yl}-morpholin-4-yl-methanoneHCID 167542529.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-aza-bicyclo[3.1.0]hexane hydrochloride (example 4 step 7, 49 mg, 1.2 eq.) and potassium carbonate (118 mg, 2.5 eq.) in acetonitrile was stirred 1 h at 60° C. The reaction mixture was cooled to 30° C. and [5-(3-chloro-propoxy)-1H-indol-2-yl]-morpholin-4-yl-methanone (example 4, step 3, 110 mg, 1.0 eq.) was added. The resulting mixture was stirred 24 h at 80° C. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with an aqueous solution of sodium hydrogencarbonate and water and dried over sodium sulphate and evaporated in vacuo. The residue was purified on silica, eluting with a 98:2 to 9:1 gradient of dichloromethane/methanol, to yield 12 mg (8%) of the desired product as light yellow solid. MS (m/e): 370.4 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388095B2
Source datasetuspto-grants-2008_06
ORD IDord-b63192ca715d46cca4cf20bad06bcf06
Source noteuspto-grants-2008_06