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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1809575생성일: 2026년 10월 27일

Tert-butyl 4-(5-(3-phenoxy-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate → 3-Phenoxy-N-(3-(piperidin-4-yl)-1,2,4-thiadiazol-5-yl)-5-(pyridin-2-ylthio)pyridin-2-amine

https://huagongshe.com/reaction/1809575

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 4-(5-(3-phenoxy-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylateHCID 57742666—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
용매Dichloromethane methanolHCID 21226129—
생성물3-Phenoxy-N-(3-(piperidin-4-yl)-1,2,4-thiadiazol-5-yl)-5-(pyridin-2-ylthio)pyridin-2-amineHCID 5774279298.3%

반응 단계

Tert-butyl 4-(5-(3-phenoxy-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)piperidine-1-carboxylate (0.587 g, 1.04 mmol) was dissolved in 1:1 CH2Cl2/methanol and 4N HCl in dioxane was added and stirred at ambient temperature for 1 hour. The reaction was concentrated and dried in vacuum oven. The HCl salt was partitioned between 5% MeOH in CH2Cl2 and saturated aqueous sodium bicarbonate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated to give N-(3-phenoxy-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(piperidin-4-yl)-1,2,4-thiadiazol-5-amine (0.473 g, 98.0% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362037B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-9fbc988b34b9462bbaf7cce86eced764
출처 메모uspto-grants-2013_01