HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723438Generated: October 26, 2026
Potassium Iodide → N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine
https://huagongshe.com/reaction/1723438
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide | HCID 14575275 | — |
| Reactant | [2-(4-Methoxyphenyl)ethyl]methanesulfonate | HCID 20025614 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine | HCID 14575764 | 41% |
Reaction Steps
A mixture of 2.3 parts of [2-(4-methoxyphenyl)ethyl]methanesulfonate, 4 parts of N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide was stirred overnight at 70° C. The reaction mixture was poured onto water and the product was extracted with methylbenzene. The extract was washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.5 parts (41%) of N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine; mp. 142.5° C. (178).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04861785 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-7a0c2a3aee01487a870b508bdb2b4629 |
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| Source note | uspto-grants-1989_08 |
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