HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(aminomethyl)-N-[4-[[5-(4-phenylphenyl)pyrazolo[1,5-c]pyrimidin-7-yl]amino]phenyl]benzamide;2,2,2-trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | {4-[4-(5-Biphenyl-4-yl-pyrazolo[1,5-c]pyrimidin-7-ylamino)-phenylcarbamoyl]benzyl}-carbamic acid tert-butyl ester | HCID 67319580 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(aminomethyl)-N-[4-[[5-(4-phenylphenyl)pyrazolo[1,5-c]pyrimidin-7-yl]amino]phenyl]benzamide;2,2,2-trifluoroacetic acid | HCID 86616043 | — |
Reaction Steps
A mixture of {4-[4-(5-biphenyl-4-yl-pyrazolo[1,5-c]pyrimidin-7-ylamino)-phenylcarbamoyl]benzyl}-carbamic acid tert-butyl ester (compound A1)(0.14 g) and trifluoroacetic acid (TFA)(1 ml) in dichloromethane (5 ml) is stirred 3 h at ambient temperature. The reaction mixture is evaporated, coevaporated with toluene and dried at high vacuum. Colorless crystals (0.13 g) are obtained in quantitative yield and a transition temperature of 170° C. and a melting temperature at 230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745446B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8c10bb483e854cf5bfa1ed7977140ae4 |
| Source note | uspto-grants-2010_06 |