HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoindane → 7-(2-Indanylamino)oxazolo[5,4-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Reactant | HCID 54245542 | HCID 54245542 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-(2-Indanylamino)oxazolo[5,4-d]pyrimidine | HCID 22719608 | 14.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703421B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-f1e198aa232043b4960ed8b5e29ac696 |
| Source note | uspto-grants-2004_03 |