HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-bromo-2-chloro-5-fluoro-N-(1-methyl-4-piperidyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 4-Bromo-2-chloro-5-fluorobenzoic acid | HCID 2736225 | — |
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-bromo-2-chloro-5-fluoro-N-(1-methyl-4-piperidyl)benzamide | HCID 68680732 | 82% |
Reaction Steps
4-bromo-2-chloro-5-fluoro-benzoic acid (Apollo Scientific; 5.0 g, 19.8 mmol) was added to DMF (250 mL), to this was added HBTU (9.8 g, 25.7 mmol), N-methyl-4-aminopiperidine (Fluorochem; 2.5 g, 21.8 mmol) and DIPEA (7.0 mL, 39.5 mmol). The reaction was stirred overnight, evaporated to dryness, quenched with 2.0 N NaOH (100 mL), extracted with DCM (3×100 mL), dried and solvent removed in vacuo. The residue was dissolved in hot acetonitrile, allowed to cool filtered, and the filtrate passed through a SCX column and the residue, after evaporation of product containing fractions, recrystallised from hot acetonitrile to yield the title compound as a white solid (5.0 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709471B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1948032135f6477d9bd7212da31890f4 |
| Source note | uspto-grants-2010_05 |