HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → N-((1-benzyl-4-hydroxypiperidin-4-yl)methyl)-2-chloroacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Aminomethyl)-1-benzylpiperidin-4-ol | HCID 10421026 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-((1-benzyl-4-hydroxypiperidin-4-yl)methyl)-2-chloroacetamide | HCID 52911160 | 78.4% |
Reaction Steps
To a solution of compound 397 (39.7 g, 180 mmol) in dichloromethane (350 mL) was added triethylamine (50.0 mL, 359 mmol), followed by dropwise addition of chloroacetyl chloride (16.5 mL, 207 mmol) over 15 minutes. The resulting solution was stirred at room temperature for 1.25 hours. The crude mixture was diluted with DCM and water, and extracted with DCM twice. The combined organics were dried over Na2SO4 and concentrated in vacuo to give compound 398 (41.9 g, 78%). LCMS-ESI (POS), M/Z, M+1: Found 297.1, Calculated 297.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841312B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7125caf86ff74a11ba1481bce2255e20 |
| Source note | uspto-grants-2014_09 |