HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (S)-1-(7-Fluoro-1-phenyl-1H-benzo[D]imidazol-2-YL)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | [(S)-1-(7-Fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tertbutyl ester | HCID 68157602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-1-(7-Fluoro-1-phenyl-1H-benzo[D]imidazol-2-YL)ethanamine | HCID 68157214 | 83% |
Reaction Steps
To a solution of [(S)-1-(7-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid tertbutyl ester (625 mg) in DCM (3 mL) was added TFA (3 mL) and the resulting mixture was stirred at RT for 3 h. The crude reaction mixture was loaded onto an Isolute® SCX-2 cartridge. The cartridge was washed with MeOH and the product eluted with 2M NH3/MeOH. The product containing fractions were combined and concentrated in vacuo affording (S)-1-(7-Fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethylamine as a pale orange oil (372 mg, 83%). LCMS: RT 1.97 and 2.11 min [M+H]+ 255.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-872b8c15a7ce401d9ce3842897fc6af4 |
| Source note | uspto-grants-2014_02 |