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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazine | HCID 595673 | — |
| Reactant | 6,7-dimethoxy-3,4-dihydro-2H-1lambda6,2,4-benzothiadiazine-1,1,3-trione | HCID 13650560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-6,7-dimethoxy-3,4-dihydro-1,2,4-benzothiadiazine-3-one 1,1-dioxide | HCID 13650561 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04716161 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-7b775669e1914ccda2b9c42056784f01 |
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| Source note | uspto-grants-1987_12 |
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