Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 5-amino-1-beta-D-ribofuranosyl-4-cyanoimidazole | HCID 10977550 | — |
| Solvent | Ammonia methanol | HCID 21705897 | — |
| Product | 2-Methyladenosine | HCID 459890 | 35.9% |
Reaction Steps
10 g of 5-amino-1-β-D-ribofuranosyl-4-imidazolecarbonitrile was dissolved in 20% ammonia methanol solution. 10 ml of acetonitrile was added thereto and the solution was heated for 5 hours at 180° C. The solvent was distilled off, purified by silica gel column chromatography and recrystallized from methanol to give 4.2 g of 2-methyladenosine (yield: 35.9%). 2-methyladenosine was methylated in the same manner as the above-mentioned [METHOD 1] to give Compound 5 and Compound 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04843066 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-ad34449c2e004f64811a41dcface1a3e |
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| Source note | uspto-grants-1989_06 |
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