HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-chloro-9-ethyl-6-(3-cyano-phenyl-amino)-9H-purine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 21988299 | HCID 21988299 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-chloro-9-ethyl-6-(3-cyano-phenyl-amino)-9H-purine | HCID 21988273 | — |
Reaction Steps
1.5 g (3.95 mmol) of 2-chloro-6-(3-cyano-phenyl-amino)-purine, 2.1 g (6.3 mmol) of caesium carbonate and 2.6 ml (31.6 mmol) of iodoethane are stirred in 66 ml of a mixture comprising dioxane:water:DMF in a ratio of 1:2:3 at RT for 19 h. Thereafter, the reaction mixture is diluted with ethyl acetate and the organic phase is washed with water. After drying over sodium sulfate, the residue is chromatographed over silica gel (mobile phase: ethyl acetate:hexane=4:1). After removal of the solvent, 2-chloro-9-ethyl-6-(3-cyano-phenyl-amino)-9H-purine is obtained as a crystalline precipitate. This precipitate is filtered off and dried; m.p. 189° C.; FAB-MS: (M+H)+=299; Rf=0.9 (CH2Cl2:methanol 9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091346B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-b125fb03c3bd4ad09878ca15f280ae05 |
| Source note | uspto-grants-2006_08 |