HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-amino-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-[[(2,3-Difluorophenyl)methyl]thio]-5-nitroso4,6-pyrimidinediamine | HCID 22288499 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-amino-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinone | HCID 22320081 | — |
Reaction Steps
To a solution of triethyl phosphonoacetate (15.0 g) in tetrahydrofuran (60 ml) cooled in an ice bath was added butyllithium (2.5M in hexanes, 25.6 ml) at a rate such that the internal temperature was maintained below 30° C. To this mixture was then added a solution of the product of Example 2 step (b) (10.0 g) in N,N-dimethylformamide (60 ml). The reaction mixture was heated at reflux for 1 hour, then cooled to room temperature and quenched with acetic acid (6 ml). The solid thus precipitated was isolated by filtration, washed with water, ethanol and diethyl ether, and dried over P2O5 at 50° C. to give the sub-titled product as a pale green solid (9.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579342B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-6010ac03a6534edcb73ddbc62b6bbd56 |
| Source note | uspto-grants-2009_08 |