Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Purine | HCID 1044 | 188.8% |
Reaction Steps
In a 100 ml three-mouth bottle, 2,6-dichloropurine (10 g), ethyl acetate (50 ml), pyridinium salt of paratoluenesulfonic acid (0.2 g) are mixed. The above mixture is stirred and heated to a temperature of 35° C., 2,3-dihydropyrane (12 ml) is added thereto within 5 min. The above mixture is reacted at 50˜60° C. for 3 h. The completion of reaction is checked with TCL analysis. Methylpiperazine (9.0 g) and triethylamine (8 ml) are added to the bottle. The above mixture is reacted at the temperature for 1 h. The completion of reaction is checked with TCL analysis. The reaction mixture is cooled to room temperature. After filtration, a filter cake is completely washed with ethyl acetate, and a filtrate is washed with water for 3 times and delaminated. Organic layer is concentrated till large amount of solid is separated out. After filtration, a filter cake is washed with ethyl acetate for 3 times and then dried in vacuum for 5 h at to obtain solid purin (12.0 g). The yield is about 67.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580763B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-cc3927e6c9fc46fbbdf11776f26cab34 |
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| Source note | uspto-grants-2013_11 |
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