HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624080Generated: October 31, 2026
Trifluoroacetic acid → rac-N-(1-(pyrrolidin-2-ylmethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide
https://huagongshe.com/reaction/624080
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | rac-tert-butyl 2-((4-(5-(m-tolyl)oxazole-4-carboxamido)-1H-pyrazol-1-yl)methyl)pyrrolidine-1-carboxylate | HCID 131735188 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | rac-N-(1-(pyrrolidin-2-ylmethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide | HCID 123442042 | — |
Reaction Steps
To a solution of rac-tert-butyl 2-((4-(5-(m-tolyl)oxazole-4-carboxamido)-1H-pyrazol-1-yl)methyl)pyrrolidine-1-carboxylate (100 mg, 0.22 mmol) in DCM (2.3 mL), TFA (0.170 mL, 2.215 mmol) was added at 0° C. After stirring for 5 h at rt, the solvent and the remaining TFA was removed under reduced pressure. The residue was dissolved in DCM and 1 N aq. NaOH-solution was added until basic. The layers were separated and the aq. layer was extracted with DCM (1×). The combined organic layers were washed with brine, dired (MgSO4), filterd and the solvent was removed under reduced pressure to yield rac-N-(1-(pyrrolidin-2-ylmethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide a yellow oil which was used in the next step without further purification. LC-MS conditions A: tR=0.62 min, [M+H]+=352.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09303023B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-e15c84ff30e64aeab32eb2266593a3db |
|---|
| Source note | uspto-grants-2016_04 |
|---|