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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9133생성일: 2026년 10월 25일

1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea → 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9133

반응식

참여 물질

역할이름HCID투입량
반응물1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylureaHCID 21985545—
촉매Lindlars catalystHCID 131709914—
용매EthanolHCID 702—
생성물1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylureaHCID 8658897341%

반응 단계

A suspension of 1-(6-phenylacetylenyl-2-benzothiazolyl)-3-ethylurea (0.032 g, 83% purity by weight, 0.083 mmol) and Lindlar catalyst (0.030 g, 5% weight purity, 0.012 mmol, 0.15 eq) in 2 mL ethanol was purged with nitrogen gas, followed by bubbling of hydrogen gas. It was stirred under hydrogen atmosphere for about 36 hours. The mixture was taken up in 10 mL MeOH, filtered, concentrated, and purified by preparative TLC to give 0.011 g (41%) of the desired compound. LC/MS 324 (M+1); LC retention time 2.84 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b034843c1eae49b58ee346d1b1960c87
출처 메모uspto-grants-2006_08