Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48406Generated: October 29, 2026

2-Aminoindane → 7-(2-Indanylamino)oxazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/48406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoindaneHCID 76310—
ReactantHCID 54245542HCID 54245542—
SolventEthanolHCID 702—
Product7-(2-Indanylamino)oxazolo[5,4-d]pyrimidineHCID 2271960814.7%

Reaction Steps

4-cyano-5-ethoxymethyleneaminooxazole (240 mg, 1.5 mmol) (see, J. Am. Chem. Soc., 88, 3829 (1966), Bull. Chem. Soc. JAPAN, 43, 187 (1970), Bull. Chem. Soc. JAPAN, 43, 3909 (1970)) and 2-aminoindan (580 mg, 4.4 mmol) in dry ethanol (2 ml) were heated to reflux for 6.5 hours. The residue obtained by distilling off the solvent under reduced pressure was purified by silica gel chromatography (methylene chloride:ethyl acetate=1:4) to obtain the title compound (56 mg, 0.22 mmol) having the following physical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703421B1
Source datasetuspto-grants-2004_03
ORD IDord-f1e198aa232043b4960ed8b5e29ac696
Source noteuspto-grants-2004_03