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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4503생성일: 2026년 10월 24일

Pyridine → morpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate

https://huagongshe.com/ko/reaction/4503

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물PhosgeneHCID 6371—
반응물Mycophenolate MofetilHCID 5281078—
용매BenzeneHCID 241—
생성물morpholinoethyl E-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoateHCID 67854272—

반응 조건

온도25 °C

반응 단계

To a solution of 500 mgs of morpholinoethyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate in 10 ml of benzene cooled in an ice bath is added 0.1 ml of pyridine and 6 ml of a 12.5% solution of phosgene in benzene. The solution is stirred at 25° C. overnight, the precipitate filtered off and solvent removed from the filtrate under reduced pressure. The residue is dissolved in 5 ml of tetrahydrofuran and to this solution is added dropwise a solution of ammonia in tetrahydrofuran until the reaction is complete. The mixture is poured into water and extracted with ethyl acetate. The organic solution is dried over magnesium sulfate and evaporated to an oil which is chromatographed on silica gel, eluting with a 50:1 mixture of dichloromethane and methanol. The purified product is stirred with a mixture of ether and hexane and filtered giving morpholinoethyl (E)-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727069
출처 데이터셋uspto-grants-1988_02
ORD IDord-ce801baf663247ddbe6aa39a88d06aae
출처 메모uspto-grants-1988_02