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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2,2-Trichloroethyl 5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenylcarbamate | HCID 68106879 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(5-tert-butyl-3-(hydroxymethyl)-2-methoxyphenyl)-3-(2,3-dihydro-1H-indene-2-yl)urea | HCID 68107401 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653304B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-1591d1f354ad4c3c8f74ce94fd7a69ac |
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| Source note | uspto-grants-2014_02 |
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