HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1761485Erstellt: 25. Oktober 2026
Dimethylformamide → 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine
https://huagongshe.com/reaction/1761485
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine | HCID 14048944 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine | HCID 21241587 | 84% |
Reaktionsschritte
A mixture of 8.7 parts of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine, 1.44 parts of a sodium hydride dispersion 60% and 270 parts of N,N-dimethylformamide was stirred for 1 hour at room temperature. 5.48 Parts of iodomethane were added dropwise slowly. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was poured into water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated in vacuo. The residue was purified by column chromatography (HPLC) over silica gel using a mixture of dichloromethane and methanol (98.75:1.25 by volume) as eluent. The second fraction was collected and the eluent was evaporated, yielding 7.6 parts (84%) of 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine as a residue (intermediate 52).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04826848 |
|---|
| Quelldatensatz | uspto-grants-1989_05 |
|---|
| ORD ID | ord-7cd75d0429bf4d87af5fa3b11ba8793d |
|---|
| Quellennotiz | uspto-grants-1989_05 |
|---|