HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 9-(2,6-Dichlorobenzyl)-6-methylaminopurine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N6-Methyladenine | HCID 67955 | — |
| Reactant | 2,6-Dichlorobenzyl chloride | HCID 74832 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 9-(2,6-Dichlorobenzyl)-6-methylaminopurine | HCID 14417383 | 62% |
Reaction Steps
In a procedure analogous to that of Example 9, by using 1.49 g of 6-methylaminopurine, 1.38 g of potassium carbonate, 50 ml of N,N-dimethylacetamide and 3.92 g of 2,6-dichlorobenzyl chloride, there was obtained 1.9 g of 9-(2,6-dichlorobenzyl)-6-methylaminopurine as colorless needles (yield: 62%), m.p. 219°-220° C. NMR spectrum of this product is identical with that of the corresponding compound synthesized in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189485 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-cb69118198f34181a2a0e1c42bbf99e2 |
| Source note | uspto-grants-1980_02 |