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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579805Generated: October 26, 2026

Sodium Iodide → 6-chloro-N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]-methyl]-2-benzothiazolamine

https://huagongshe.com/reaction/579805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromomethyl-1,4-benzodioxaneHCID 98333—
Reactant6-chloro-N-(4-piperidinylmethyl)-2-benzothiazolamine dihydrobromideHCID 21241579—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product6-chloro-N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]-methyl]-2-benzothiazolamineHCID 1404898859.8%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 1.9 parts of 2-(bromomethyl)-2,3-dihydro-1,4-benzodioxin, 3.3 parts of 6-chloro-N-(4-piperidinylmethyl)-2-benzothiazolamine dihydrobromide, 5 parts of sodium carbonate, 0.1 parts of sodium iodide and 67.5 parts of N,N-dimethylacetamide was stirred overnight at about 75° C. Water was added to the reaction mixture and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The oily residue was crystallized from a mixture of 1,1'-oxybisethane and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.8 parts (59.8%) of 6-chloro-N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]-methyl]-2-benzothiazolamine; mp. 155.8° C. (compound 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749702
Source datasetuspto-grants-1988_06
ORD IDord-8fe7211fd02c4e538dfbc26e61b2fc2b
Source noteuspto-grants-1988_06