HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoindane → 4-(2-Indanylamino)thieno[3,4-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Reactant | 4-Methylthiothieno[3,4-d]pyrimidine | HCID 10464959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Indanylamino)thieno[3,4-d]pyrimidine | HCID 22719597 | 22% |
Reaction Steps
4-methylthiothieno[3,4-d]pyrimidine (90 mg, 0.50 mmol) (see J. Heterocyclic Chem., 30, 509 (1993)) and 2-aminoindan (200 mg, 1.5 mmol) in dry ethanol (4 ml) were heated to reflux under an argon atmosphere for 4 hours. The solvent was distilled off under reduced pressure and the residue obtained was purified by silica gel chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (30 mg, 0.11 mmol) having the following physical properties;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734180B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-8e5c60da52ff4f968b51d7636f9bb65c |
| Source note | uspto-grants-2004_05 |