HuagongsheHuagongshe Chemistry Print Report · For research reference only
Purine → HCID 178420486, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Purine | HCID 1044 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178420486 | HCID 178420486 | — |
Reaction Steps
The general procedure for the synthesis of purine derivatives is depicted in FIG. 1. The initial compound 6-chloropurine (1.0 eq.) was mixed with aniline (1.20 eq.) and K2CO3 (2.5 eq.) in 50.0 ml dioxane. The resultant mixture was charged in 100 mL round bottom flask with a stirring bar. The mixture was refluxed overnight and monitored by TLC. After the reaction finished, the solvent was removed and the remaining residue was extracted by ethyl acetate. After removing the solvent, the resultant crude product was purified by silica gel column chromatography eluting with CH2Cl2/MeOH (5%) to provide pure titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193711B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-f2e117a9e6a742a3af4dcf7ebec7395a |
| Source note | uspto-grants-2015_11 |