HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-(1-(2-Aminoethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86704223 | HCID 86704223 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-(2-Aminoethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide | HCID 86704224 | — |
Reaction Steps
To a suspension of tert-butyl(2-(4-(5-(m-tolyl)oxazole-4-carboxamido)-1H-pyrazol-1-yl)ethyl)carbamate (4.29 g, 10.426 mmol) in DCM (60 mL), TFA (12 mL, 156.39 mmol) was added at 0° C. After strring for 1 h at rt, the reaction mixture was concentrated. The residue was dissolved in DCM and 2 N aq. NaOH-solution was added. The org. layer was separated and the aq. layer was extracted with DCM (2×). The combined org. layers were dried (MgSO4), filtered and the solvent removed to yield the title compound as a white solid, which was used in the next step without further purification. LC-MS conditions B: tR=0.54 min, [M+H]+=312.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303023B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c69bb5762aaa43f19e873cc4c04a9430 |
| Source note | uspto-grants-2016_04 |