HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adenine → N-(3-Thienylmethyl)-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adenine | HCID 190 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-Thenoyl chloride | HCID 2776377 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(3-Thienylmethyl)-9H-purin-6-amine | HCID 13536440 | — |
Reaction Steps
In the other version of the process, 1 mole equivalent of adenine is heated in a conventional manner (Phytochemistry 16, (1977) 1865) with from 1 to 10, preferably from 2 to 5, mole equivalents of thiophene-3-carbonyl chloride in the presence of a proton acceptor (e.g. pyridine), possibly in a solvent, such as dioxane, at as high as 200° C., and the mixture is worked up in a conventional manner and if necessary recrystallized, for example as described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04718936 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-d1e2bd802d7149e38e0b052534c4a447 |
| Source note | uspto-grants-1988_01 |