HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfur, trifluoro(N-methylmethanaminato)- → HCID 23505756, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfur, trifluoro(N-methylmethanaminato)- | HCID 123203 | — |
| Reactant | HCID 23505732 | HCID 23505732 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23505756 | HCID 23505756 | — |
Reaction Steps
A solution of {4-[4-(butyl-ethyl-amino)-2,5-dimethyl-pyrrolo[2,3-d]pyrimidin-7-yl]-3,5-dimethylphenyl}-methanol (0.071 g, 0.186 mmol) in 2 ml anhydrous methylene chloride was cooled to −78° C. and treated with dimethylaminosulfur trifluoride (0.063g, 0.390 mmol) and stirred at room temperature for 1 hour. The mixture was quenched with water and extracted with chloroform. The organic layer was washed with brine, dried, and concentrated to give an oil which was purified through silica gel using 2% methanol/chloroform as eluent to give the title compound as an off-white solid, mp 163-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06765008B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-cd398e5afb0e445e80dd7eb0f008f48b |
| Source note | uspto-grants-2004_07 |