HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789495Generated: October 25, 2026
Dimethylformamide → 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine
https://huagongshe.com/reaction/1789495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine | HCID 14048944 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine | HCID 21241587 | 84% |
Reaction Steps
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 faction 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689330 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-8ac978557b4942dd8db7d2fbfc8ff579 |
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| Source note | uspto-grants-1987_08 |
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