HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178522645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | HCID 178509243 | HCID 178509243 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178522645 | HCID 178522645 | — |
Reaction Steps
To a solution of 6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-3-ylamine (45 mg, 0.17 mmol) in 1.7 mL of dioxane was added 14 uL pyridine and cyclopropane carbonyl chloride (21 uL, 0.17 mmol). The reaction mixture was heated to reflux for three hours, then cooled and chromatographed through silica (20%-50% EtOAc in hexanes) to afford 32 mg of cyclopentanecarboxylic acid [6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-amide, MP=206.3-207.51° C., MS (M+H)=360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601726B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-cbbda30b7529477581803e3735cf113a |
| Source note | uspto-grants-2009_10 |