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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356957Generated: November 1, 2026

Diphosgene → 3-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-6-yl)-5,5-dimethyl-1-pyridin-4-ylmethyl-imidazolidine-2,4-dione

https://huagongshe.com/reaction/2356957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphosgeneHCID 10426—
Reactant1-(6-Amino-3,3-dimethylindolin-1-yl)ethanoneHCID 21865176—
ReactantHCID 43725938HCID 43725938—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-6-yl)-5,5-dimethyl-1-pyridin-4-ylmethyl-imidazolidine-2,4-dioneHCID 66915806—

Reaction Steps

7.26 g (36.7 mmol) of diphosgene were initially charged at −20° C. in 80 ml of 1,2-dichloroethane, and 3.0 g (14.5 mmol) of 1-(6-amino-3,3-dimethyl-2,3-dihydroindol-1-yl)ethanone, dissolved in 80 ml of 1,2-dichloroethane, were added dropwise. After stirring at RT for 2 h and reflux for 1 h, the mixture was concentrated fully. The remaining residue was dissolved in 80 ml of THF, added to a solution of 3.06 g (14.7 mmol) of methyl 2-methyl-2-[(pyridin-4-ylmethyl)amino]propionate in 80 ml of THF, and heated under reflux for 8 h. The residue remaining after evaporation was purified by means of preparative HPLC (RP18, acetonitrile/water, 0.1% TFA). Yield: 4.69 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759379B2
Source datasetuspto-grants-2010_07
ORD IDord-8618c24646224636a7e831ecbd9196dc
Source noteuspto-grants-2010_07