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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507591Generated: October 31, 2026

Potassium Carbonate → 6-Amino-1-(3-cyclopropoxypropyl)-3,3-dimethylindolin-2-one

https://huagongshe.com/reaction/1507591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
ReactantL-ProlineHCID 145742—
Reactant6-Bromo-1-(3-cyclopropoxypropyl)-3,3-dimethylindolin-2-oneHCID 90046350—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Solventtert-Butyl methyl etherHCID 15413—
Product6-Amino-1-(3-cyclopropoxypropyl)-3,3-dimethylindolin-2-oneHCID 90046308—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of 6-bromo-1-(3-cyclopropoxypropyl)-3,3-dimethylindolin-2-one (360 mg, 1.06 mmol) and K2CO3 (441 mg, 3.19 mmol) in DMSO (2 ml) were added L-proline (49.0 mg, 426 μmol), copper (I) iodide (40.5 mg, 213 μmol) and ammonium hydroxide (373 mg, 414 μl, 2.66 mmol). The tube was sealed and heated to 90° C. for 7 hours. The reaction mixture was poured into TBME (50 ml) and extracted with 1 M HCl. The combined aqueous layers were basified with 2M Na2CO3. The aqueous phase was extracted two times with TBME. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The title compound was obtained as brown viscous oil (228 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221816B2
Source datasetuspto-grants-2015_12
ORD IDord-580bec4e990445e38b623f3763bcc4de
Source noteuspto-grants-2015_12