Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 59603829 | HCID 59603829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59603901 | HCID 59603901 | 51.8% |
Reaction Steps
4-[6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidin-3-yl]-N-(2,2,2-trifluoroethyl)thiophene-2-carboxamide (107 mg, 0.263 mmol) was taken up in thionyl chloride (2 ml, 27.4 mmol) and heated at 80° C. overnight. Evaporated solvent under vacuum and took up in 3 ml DMF, purified reverse-phase 30-100% ACN/H2O w/0.1% TFA. Evaporated solvent under vacuum to yield 60 mgs pale yellow solid (51.7%). LRMS [M+H]=441.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08461162B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-8638fdc834c742a69bad6539d9a819d7 |
|---|
| Source note | uspto-grants-2013_06 |
|---|