HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-chloro-N-(1-methyl-4-piperidyl)-4-nitro-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | 3-Chloro-4-nitrobenzoyl chloride | HCID 19077614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-chloro-N-(1-methyl-4-piperidyl)-4-nitro-benzamide | HCID 68686719 | 60.5% |
Reaction Steps
3-chloro-4-nitro-benzoyl chloride (Intermediate 54; 2.2 g, 10.00 mmol) was dissolved in DCM (20 mL) and N,N-diisopropylethylamine (2.095 mL, 12.00 mmol) added. The mixture was cooled in an ice/water bath and 4-amino-1-methylpiperidine (Fluorochem; 1.14 g, 10.00 mmol) in DCM (10 mL) added dropwise. The mixture was allowed to warm to room temperature and stirred for 0.5 hr. A white precipitate resulted. The reaction mixture was washed with 2N NaOH, filtered and the filter cake washed with water and dried on a sinter over the weekend to give the title compound as a white solid (1.80 g, 60%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709471B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-d8a0ad712d5e4d69b2978c7dce6a23db |
| Source note | uspto-grants-2010_05 |