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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantN-(4-piperidinyl)-2-benzothiazolamine dihydrobromideHCID 14575275—
Reactant[2-(4-Methoxyphenyl)ethyl]methanesulfonateHCID 20025614—
SolventDimethylformamideHCID 6228—
ProductN-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamineHCID 1457576441%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861785
Source datasetuspto-grants-1989_08
ORD IDord-7a0c2a3aee01487a870b508bdb2b4629
Source noteuspto-grants-1989_08