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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569576Generated: October 25, 2026

2-Chloro-6-(1-piperazinyl)pyrazine → 2-[4-[4-(6-chloro-2-pyrazinyl)-1-piperazinyl]butyl]-3a,4,7,7a-tetrahydro-5,6-dimethyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide, dihydrochloride

https://huagongshe.com/reaction/569576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-(1-piperazinyl)pyrazineHCID 107992—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant3a,4,7,7a-tetrahydro-5,6-dimethyl-1,2-benzisothiazol-3-(2H)-one 1,1-dioxideHCID 12477038—
Product2-[4-[4-(6-chloro-2-pyrazinyl)-1-piperazinyl]butyl]-3a,4,7,7a-tetrahydro-5,6-dimethyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide, dihydrochlorideHCID 88521857—

Reaction Steps

The title compound is prepared using the procedure of Example 1 using 3a,4,7,7a-tetrahydro-5,6-dimethyl-1,2-benzisothiazol-3-(2H)-one 1,1-dioxide instead of 3a,4,7,7a-tetrahydro-4,7-methano-1,2-benzisothiazol-3(2H)-one 1,1-dioxide and 1-(6-chloro-2-pyrazinyl)piperazine instead of 4-(2-pyrimidinyl)piperazine. The final product is converted to its dihydrochloride salt, mp 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732984
Source datasetuspto-grants-1988_03
ORD IDord-4931d279d7594679a4d32efc8e4fd4c1
Source noteuspto-grants-1988_03