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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9138생성일: 2026년 10월 24일

Methanol → 1-(6-(3-Aminopropanoyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/ko/reaction/9138

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물1-(6-(2-Cyanoacetyl)-2-benzothiazolyl)-3-ethylureaHCID 21985554—
촉매Adams' catalystHCID 345198—
용매ChloroformHCID 6212—
생성물1-(6-(3-Aminopropanoyl)-2-benzothiazolyl)-3-ethylureaHCID 21985556121.5%

반응 단계

A suspension of 1-(6-(2-cyanoacetyl)-2-benzothiazolyl)-3-ethylurea (0.56 g, 1.94 mmol) and platinum (IV) oxide (0.176 g, 0.78 mmol, 0.40 eq) in 50 mL of 2/3 mixture of MeOH and chloroform was purged and bubbled with hydrogen gas. It was stirred under hydrogen gas for about 2 days. The mixture was filtered and concentrated to give 0.689 g (quantitative yield) desired compound. LC/MS 292.9 (M+1); LC retention time 1.80 min. HPLC purification gave corresponding acetic acid salt. LC/MS 292.9 (M+1); LC retention time 1.80 min. In a similar reaction, compound as an acetate salt form was obtained after HPLC purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ec7552d657b74d9cb90ee4e75ae57522
출처 메모uspto-grants-2006_08