HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-amino-N-(1-methylpiperidin-4-yl)-3-(trifluoromethoxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-amino-3-(trifluoromethoxy)benzoic Acid | HCID 2735951 | — |
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Product | 4-amino-N-(1-methylpiperidin-4-yl)-3-(trifluoromethoxy)benzamide | HCID 58015152 | 71% |
Reaction Steps
To a suspension of 4-amino-3-(trifluoromethoxy)benzoic acid (900 mg, 4 mmol) in dichloromethane (60 ml) TBTU (1.9 g, 6 mmol) and DIPEA (1.04 ml, 6 mmol) were added. The mixture was stirred at room temperature for 30 minutes. Then 1-methylpiperidin-4-amine (513 mg, 4.5 mmol) was added and the reaction was stirred for an additional 3 h. The solution was washed with water and the organic phase was dried over anhydrous Na2SO4. The crude was purified by flash chromatography (DCM/MeOH/NH3aq, 9:1:0.5), to give the title compound (900 mg, 71%), as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08614220B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-3e5600baa2c8498ea0eb3752c04771d8 |
| Source note | uspto-grants-2013_12 |