Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indan-5-amine | HCID 90496 | — |
| Reactant | HCID 21839576 | HCID 21839576 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21839590 | HCID 21839590 | 40% |
Reaction Steps
A suspension of 4-(5-indanylthio)-pyrido[2,3-d]pyrimidine (2.79 g, 10 mM) and 5-aminoindan (3.996 g, 30 mM) in water (100 ml) is heated in a sealed tube at 130° C. for 20 h. Then the water is evaporated under vacuum and the residue chromatographed on silica gel by using dichloromethane/methanol mixtures as eluant. Thus almost pure title compound is obtained in about 40% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965563 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-1e9239a3eee9457486adc712a97de27b |
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| Source note | uspto-grants-1999_10 |
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