Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 20029971 | HCID 20029971 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20029986 | HCID 20029986 | 82% |
Reaction Steps
A mixture of 8.5 g. (22 mmole) 6-(N-allyl-N-cyclohexylamino)-2-chloro-9-tetrahydrofuran-2-ylpurine and 150 ml. methanol, which has been saturated with methylamine, is heated to 100° C. in an autoclave for 48 hours. The reaction mixture is then evaporated, the residue is taken up in dichloromethane, washed with water, dried and evaporated. After chromatography with dichloromethane, there are obtained 6.4 g. of the title compound (82% of theory) in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853386 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-a7b0c86d791740e1baa9d745e69317af |
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| Source note | uspto-grants-1989_08 |
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