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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400145생성일: 2026년 10월 25일

2,2-Dimethylvaleroyl chloride → (4R,6R)-6-{2-[(1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-Hexahydro-6-t-butyldimethylsilyloxy-8-(2,2-dimethylvaleryloxy)-2-methyl-1-naphthyl]ethyl}tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-one

https://huagongshe.com/reaction/400145

반응식

참여 물질

역할이름HCID투입량
반응물2,2-Dimethylvaleroyl chlorideHCID 519171—
반응물Pravastatin Diol Lactone Di-(tert-butyldimethylsilyl) EtherHCID 14600906—
생성물(4R,6R)-6-{2-[(1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-Hexahydro-6-t-butyldimethylsilyloxy-8-(2,2-dimethylvaleryloxy)-2-methyl-1-naphthyl]ethyl}tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-oneHCID 5379604854.9%

반응 단계

A procedure similar to that described in Example 4, above, was followed, but using 2.0 g (3.6 mmol) of (4R,6R)-6-{2-[(1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-hexahydro-6-t-butyldimethylsilyloxy-8-hydroxy-2-methyl-1-naphthyl]ethyl}tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-one [prepared as described in Example B, above] and 2.16 g (14.5 mmol) of 2,2-dimethylpentanoyl chloride, to provide 1.31 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05827855
출처 데이터셋uspto-grants-1998_10
ORD IDord-76409f53ba6d4acd898ef8c5ccbc9d14
출처 메모uspto-grants-1998_10