Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Chloro-6-methyl-8-propylpurine | HCID 19012212 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19012209 | HCID 19012209 | — |
Reaction Steps
To a solution of 2-Chloro-6-methyl-8-propylpurine (from Step 1 of Example 32) (0.1 g, 0.47 mmol) in ethanol (2 ml) was added condensed methylamine (1 ml) at -20° C. The mixture was then placed in a steel-bomb and heated at 110° C. for 7 hours. The reaction was cooled and the mixture was concentrated in vacuo. The residue was partitioned between CHCl3 and water, and the organic layer was separated and dried over MgSO4. The crude product obtained after removal of the solvent was purified by flash-chromatography on silica-gel using 5% MeOH in CHCl3 giving the titled compound as an amorphous solid (0.115 g, quantitative). NMR (CDCl3): δ1.03 (t, J=8Hz,3H), 1.8 (q, J=8 Hz, 2H), 2.64 (s, 3H), 2.8 (t, J=8 Hz, 2H), 3.0 (d, J=5 Hz, 3H), 5.1 (br s, 1H). FAB-MS: m/e 206 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102880 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-e0df4a0c2ce24f7787ad7c491681607b |
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| Source note | uspto-grants-1992_04 |
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