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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581971Generated: October 30, 2026

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

https://huagongshe.com/reaction/1581971

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 numberUS06734180B1
Source datasetuspto-grants-2004_05
ORD IDord-d6166fb11d0e4d8c998ccc45e64de9a5
Source noteuspto-grants-2004_05