Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243809Generated: October 27, 2026

2-Aminoindane → 1-(5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenyl)-3-(2,3-dihydro-1H-indene-2-yl)urea

https://huagongshe.com/reaction/243809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoindaneHCID 76310—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2,2-Trichloroethyl 5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenylcarbamateHCID 68106879—
SolventAcetonitrileHCID 6342—
Product1-(5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenyl)-3-(2,3-dihydro-1H-indene-2-yl)ureaHCID 68107401—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2,2,2-trichloroethyl 5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenylcarbamate (0.096 g, 0.250 mmol) and 2-aminoindane (0.033 g, 0.248 mmol) in acetonitrile (1.0 mL), N,N-diisopropylethylamine (0.065 mL, 0.38 mmol) was added, and the mixture was stirred at 70° C. for 12 hours. The reaction mixture was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=0/100-60/40) to obtain 0.092 g (quantitative) of the captioned compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653304B2
Source datasetuspto-grants-2014_02
ORD IDord-1591d1f354ad4c3c8f74ce94fd7a69ac
Source noteuspto-grants-2014_02