Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986742Generated: October 25, 2026

Water → 2-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-6,7-dimethoxy-3,4-dihydro-1,2,4-benzothiadiazine-3-one 1,1-dioxide

https://huagongshe.com/reaction/986742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazineHCID 595673—
Reactant6,7-dimethoxy-3,4-dihydro-2H-1lambda6,2,4-benzothiadiazine-1,1,3-trioneHCID 13650560—
SolventDimethylformamideHCID 6228—
Product2-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-6,7-dimethoxy-3,4-dihydro-1,2,4-benzothiadiazine-3-one 1,1-dioxideHCID 1365056136%

Reaction Conditions

Temperature80 °C

Reaction Steps

One gram and a half of 6,7-dimethoxy-3,4-dihydro-1,2,4-benzothiadiazine-3-one 1,1-dioxide was dissolved in 10 ml of dimethylformamide. After adding 280 mg of sodium hydride in 50% oil, the mixture was heated to 80° C. Then, a solution of 1.5 g of 2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl chloride in 5 ml of dimethylformamide was added dropwise to the resultant reaction liquid. After the addition was finished, the stirring was continued for 5 hours while heating at 80° C. to react. The resultant reaction mixture was poured into water to precipitate crystals. The produced crystals were filtered off followed by recrystallizing from methanol to obtain 1.0 g of the titled compound (yield: 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04716161
Source datasetuspto-grants-1987_12
ORD IDord-7b775669e1914ccda2b9c42056784f01
Source noteuspto-grants-1987_12