HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428755Generated: November 2, 2026
Trifluoroacetic acid → HCID 86680221, compound
https://huagongshe.com/reaction/1428755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86680220 | HCID 86680220 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86680221 | HCID 86680221 | 113.8% |
Reaction Steps
To a stirred solution of tert-butyl 2-methoxy-4-(1-oxo-1-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methylamino)propan-2-yl)benzylcarbamate (161 mg, 0.29 mmol) in dichloromethane (4 mL), cooled to 0° C., were added trifluoroacetic acid (2 mL). The resulting reaction mixture was stirred for 2 h at 0° C. and 2 h at room temperature, then basified to pH 8-9 with aq. NaHCO3. The mixture was filtered using celite pad. The filtrate dissolved in dichloromethane and extracted with NaHCO3. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(4-(Aminomethyl)-3-methoxyphenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (151 mg) was obtained as 99% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08937092B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-471b2411abe94ffd9b0e29b51626473e |
|---|
| Source note | uspto-grants-2015_01 |
|---|