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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1862495생성일: 2026년 10월 27일

Dithiaoctanediol → Z-(S)-[1-(2-{4-[3-(4-Chloro-phenyl)-allyloxy]-3-methoxy-phenyl}-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid-tert.-butyl ester

https://huagongshe.com/reaction/1862495

반응식

참여 물질

역할이름HCID투입량
반응물DithiaoctanediolHCID 78904—
반응물(S)-[1-(2-{4-[3-(4-chloro-phenyl)-prop-2-ynyloxy]-3-methoxy-phenyl}ethylcarbamoyl)-2-methyl-propyl]-carbamic acid-tert.-butyl esterHCID 22982866—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물Z-(S)-[1-(2-{4-[3-(4-Chloro-phenyl)-allyloxy]-3-methoxy-phenyl}-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid-tert.-butyl esterHCID 69822741—

반응 단계

To (S)-[1-(2-{4-[3-(4-chloro-phenyl)-prop-2-ynyloxy]-3-methoxy-phenyl}ethylcarbamoyl)-2-methyl-propyl]-carbamic acid-tert.-butyl ester (18 g) in tetrahyrofuran (180 ml), Lindlar-catalyst (5%-Pd on CaSO4; 7.2 g), 3,6-dithia-1,8-octandiol (45 mg) and 2,2′-(ethylenedithio)-diethanol (45 mg) are added. The resulting mixture is shaken under a hydrogen atmosphere at room temperature and at normal pressure for 5 hours. It is then filtered and evaporated. The residue is purified by flash column chromatography on silica gel (ethyl acetate/hexane 1:2) and recrystallised (ethyl acetate/hexane). Z-(S)-[1-(2-{4-[3-(4-Chloro-phenyl)-allyloxy]-3-methoxy-phenyl}-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid-tert.-butyl ester is obtained, m.p. 82-84° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06538016B2
출처 데이터셋uspto-grants-2003_03
ORD IDord-2583a6e03fc3407cadc8fc825412acc5
출처 메모uspto-grants-2003_03