HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → thieno[2,3-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chlorothieno[2,3-d]pyrimidine | HCID 736618 | — |
| Reactant | HCID 178435178 | HCID 178435178 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | thieno[2,3-d]pyrimidin-4-amine | HCID 4269486 | — |
Reaction Steps
An amine (VIII) is added to a solution of the 4-chlorothieno[2,3-d]pyrimidine (VII) in either ethanol or a mixture of acetonitrile and a base (for example an alkaline carbonate or diisopropylethylamine) in a closable bottle. The bottle is closed with a polypropylene cap, and heated overnight in a conventional oven at a temperature comprised between 40° and 120° C., preferably between 60 and 85° C. After cooling, the solvent is removed under reduced pressure, and the residue is purified by flash chromatography to provide the final thieno[2,3-d]pyrimidin-4-ylamine (I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662814B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-d4931da115324a31a67ccb56a1bffee0 |
| Source note | uspto-grants-2010_02 |