HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(2-Amino-2-phenyl-acetyl)-morpholine-3-carboxylic acid {4-[3-(5-chloro-2-hydroxy-phenyl)-1-methyl-1H-pyrazol-4-ylethynyl]-phenyl}-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | [2-(3-{4-[3-(5-Chloro-2-hydroxy-phenyl)-1-methyl-1H-pyrazol-4-ylethynyl]-phenylcarbamoyl}-morpholin-4-yl)-2-oxo-1-phenyl-ethyl]-carbamic acid tert-butyl ester | HCID 136346688 | — |
| Product | 4-(2-Amino-2-phenyl-acetyl)-morpholine-3-carboxylic acid {4-[3-(5-chloro-2-hydroxy-phenyl)-1-methyl-1H-pyrazol-4-ylethynyl]-phenyl}-amide | HCID 136346689 | 85% |
Reaction Steps
To a solution of compound 8D was slowly added TFA (20 eq). The reaction mixture was stirred at rt till all the compound 8D was reacted (4-5 h, checked with LCMS). The solvent was removed with rotavapor at 25° C. More dichloromethane was added and the solvent was removed again. The same process repeated two more times. The residua were then transferred to a separatory funnel with EtOAc and washed with saturated aqueous NaHCO3. It was dried over sodium sulfate and filtered. Solvent was removed to give the title compound 9D in >85% yield. It was used for next step without further purification. LCMS (ESI) m/z 592.34 (MNa+), 570.44 (MH+). HPLC: tR=4.27 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07923004B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-c614a417821a4915b964ef9f752a37d7 |
| Source note | uspto-grants-2011_04 |