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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22605생성일: 2026년 10월 25일

Hexane → (+)-Methyl 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoate

https://huagongshe.com/reaction/22605

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물Ammonium AcetateHCID 517165—
반응물((7-Chloroquinolin-2-yl)methyl)triphenylphosphonium bromideHCID 10391903—
반응물(+)-Methyl 5-(3-formylphenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoateHCID 19930537—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(+)-Methyl 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoateHCID 86743269—

반응 조건

온도-78 °C

반응 단계

To a suspension of 7-chloroquinolin-2-ylmethyltriphenylphosphonium bromide (809 mg, 1.56 mmol.) (Example 4, Step 2) in THF (15 mL) at -78° C., was added a solution of n-BuLi (1.6M) in hexane (0.89 mL, 1.43 mmol.). The mixture was stirred for 0.5 hrs at -78° C. Then, (-)-methyl 5-(3-formylphenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoate (step 7) (480 mg, 1.3 mmol.) in THF (4 mL) was slowly added. The mixture was stirred for 0.5 hr at -78° C. and then warmed up to room temperature and stirred for an additional 2 hrs. A solution of 25% ammonium acetate was added, the mixture was extracted with ethyl acetate, and the extracts were washed with brine (3×), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography afforded the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428171
출처 데이터셋uspto-grants-1995_06
ORD IDord-306548f89d4943a5ad95da72a0a5b8ec
출처 메모uspto-grants-1995_06