HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 58070340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-butyl N-(5-bromo-3-ethynylpyrazin-2-yl)-N-[(tert-butoxy)carbonyl]carbamate | HCID 58070394 | — |
| Reactant | 4-(Chloromethyl)-N-hydroxybenzimidoyl chloride | HCID 76686601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58070340 | HCID 58070340 | — |
Reaction Steps
Triethylamine (330.3 mg, 455.0 μL, 3.264 mmol) was added to a solution of tert-butyl N-(5-bromo-3-ethynyl-pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamate (1000 mg, 2.511 mmol) and 4-(chloromethyl)-N-hydroxy-benzimidoyl chloride 6 (563.6 mg, 2.762 mmol) in DCM (7 mL). The mixture was stirred at RT overnight. The reaction mixture was partitioned between DCM and water and the organic extract was dried (MgSO4) and concentrated in vacuo yielding an oil that was dissolved in DCM (10 mL). TFA (2 mL) was added and the mixture was stirred at RT for 15 min before being concentrated in vacuo. MS (ES−) 364
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846686B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a35c28bbddcd41b9ab43dcc9f75b3000 |
| Source note | uspto-grants-2014_09 |