돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 377163생성일: 2026년 10월 25일

4-Nitrobenzyl chloride → 3-(4-Nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one

https://huagongshe.com/reaction/377163

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrobenzyl chlorideHCID 7482—
반응물Potassium CarbonateHCID 11430—
반응물5-(3,4-Dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-oneHCID 15340822—
반응물1-(3,4-Dimethoxyphenyl)-2-bromobutan-1-oneHCID 19357910—
용매AcetoneHCID 180—
생성물3-(4-Nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-oneHCID 9801942—

반응 단계

A solution of 2.8 g of 5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one ("A") [obtainable by reacting 1-(3,4-dimethoxyphenyl)-2-bromobutan-1-one with methyl hydrazinethioformate] in 150 ml of acetone is boiled with 3 g of 4-nitrobenzyl chloride in the presence of 4 g of potassium carbonate for eight hours. The insoluble residue is filtered off and the solution is concentrated. The residue is worked up in the conventional manner to give 3-(4-nitrobenzyl)-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06025354
출처 데이터셋uspto-grants-2000_02
ORD IDord-a5cc4f3b83ea4d32b1e3a389b1a8a367
출처 메모uspto-grants-2000_02