HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylamine → N-Cyclopentyl-9-methyl-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | HCID 131719616 | HCID 131719616 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Cyclopentyl-9-methyl-9H-purin-6-amine | HCID 4401 | 74% |
Reaction Steps
To prepare N6 -cyclopenyl-9-methyl Adenine the following additional steps were taken. A mixture of 6-chloro-9-methyl Adenine (0.82 g) , cyclopentylamine (0.52 ml) , trimethylamine (0.53 ml) and ethanol. (60 ml), was refluxed for 24 hours. The solution was concentrated in vacuo to a yellow syrup. The syrup was passed through a C-18 column to give 0.78 g or 74% yield of with m.p. 108°-109° C. 1HNMR(Me2SO-d6): δ1-2 (m, 9 H); 3.7 (S, CH3); 7.6(d,NH); 8.1(S,1H); 8.2(S,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05565566 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-bb285b786787493cba191bff67f9920e |
| Source note | uspto-grants-1996_10 |