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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366427생성일: 2026년 10월 26일

1-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)piperazine → cis-7-{4-[4-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-piperazin-1-yl]-but-2-envioxy}-2-methyl-benzothiazole

https://huagongshe.com/reaction/366427

반응식

참여 물질

역할이름HCID투입량
반응물1-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)piperazineHCID 2735936—
반응물1,4-Dichloro-cis-2-buteneHCID 6432115—
반응물cis-7-(3-Chloroallyloxy)-2-methyl-benzothiazoleHCID 86755936—
생성물cis-7-{4-[4-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-piperazin-1-yl]-but-2-envioxy}-2-methyl-benzothiazoleHCID 67851631—
생성물cis-7-(3-Chloroallyloxy)-2-methyl-benzothiazoleHCID 86755936—

반응 단계

The title compound was prepared according to Method GA from cis-7-(3-chloroallyloxy)-2-methyl-benzothiazole and 1-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)piperazine. mp 114° C.; LSIMS m/z 496. The cis-7-(3-chloro-allyloxy)-2-methyl-benzothiazole was prepared by Method IV, with cis-1,4-dichloro-2-butene as the alkylating agent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130217
출처 데이터셋uspto-grants-2000_10
ORD IDord-e00a9f5c77f841b29a420b447aaf9417
출처 메모uspto-grants-2000_10