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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211141Generated: November 1, 2026

Saccharin → HCID 67809422, compound

https://huagongshe.com/reaction/2211141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSaccharinHCID 5143—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19375627HCID 19375627—
SolventDimethylformamideHCID 6228—
ProductHCID 67809422HCID 67809422—

Reaction Steps

To a stirred suspension of sodium hydride (0.31 g, 13 mmol) in 12 ml of dry DMF was added saccharin (2.29 g, 13 mmol) in 12 ml of dry DMF. Stirring was continued for 10 minutes before 1-(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)-4-(2-chloroethyl)piperazine (4.12 g, 13 mmol) (which can be obtained as described in EP-A-0190472) in 20 ml of dry DMF was added. The reaction mixture was heated under a nitrogen atmosphere for 7 hours, cooled down and extracted with ethylacetate (3×100 ml). The combined organic layers were washed with 5% NaHCO3, brine, dried and the solvent was removed in vacuo. The crude product was purified by flash column chromatography (silicagel/acetone:hexane=1:3) and the so-obtained free base was converted to its hydrochloride salt. Yield 3.13 g, (50%), m.p. 267°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462942
Source datasetuspto-grants-1995_10
ORD IDord-f8692c2f88744d3ea5aabccc5233b68c
Source noteuspto-grants-1995_10