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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1424984생성일: 2026년 10월 25일

Hydrochloric Acid → Benzyl cis(+/-)-[1-(1H-imidazol-1-ylcarbonothioyl)-3-methoxypiperidin-4-yl]-carbamate

https://huagongshe.com/reaction/1424984

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,1'-ThiocarbonyldiimidazoleHCID 80264—
반응물Benzyl cis(+/-)-[3-methoxypiperidin-4-yl]carbamateHCID 86648490—
용매TetrahydrofuranHCID 8028—
생성물Benzyl cis(+/-)-[1-(1H-imidazol-1-ylcarbonothioyl)-3-methoxypiperidin-4-yl]-carbamateHCID 86648520—

반응 단계

Benzyl cis(±)-4-(3-methoxypiperidin-4-yl)-carbamate obtained by the method described in Example (40b) (735 mg, 1.37 mmol) was dissolved in THF (8 mL). 1,1′-Thiocarbonyldiimidazole (270 mg, 1.36 mmol) was added, and the mixture was stirred for 1.5 hours. 0.5 M hydrochloric acid was added to the reaction solution, followed by extraction with ethyl acetate and dichloromethane. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927588B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-7a35a925304e45849dc88bf6112b2127
출처 메모uspto-grants-2015_01