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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1857605생성일: 2026년 10월 27일

Sodium cyanoborohydride → 7-chloro-3-(3,5-dimethylphenyl)-4-{1-[4-(4-methoxyphenyl)-butyl]-piperidin-2-yl-methoxy}-1H-quinolin-2-one

https://huagongshe.com/reaction/1857605

반응식

참여 물질

역할이름HCID투입량
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-(4-Methoxyphenyl)butanalHCID 10487555—
반응물7-chloro-3-(3,5-dimethylphenyl)-4-(piperidin-2-yl-methoxy)-1H-quinolin-2-oneHCID 22130005—
촉매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물7-chloro-3-(3,5-dimethylphenyl)-4-{1-[4-(4-methoxyphenyl)-butyl]-piperidin-2-yl-methoxy}-1H-quinolin-2-oneHCID 54032571—

반응 단계

To a solution of 7-chloro-3-(3,5-dimethylphenyl)-4-(piperidin-2-yl-methoxy)-1H-quinolin-2-one (prepared essentially as described in Example 10, 34 mg in 3.0 mL dry methanol) was added 18 mg of 4-(4-methoxyphenyl)-butyraldehyde, 150 mg powdered 4 Å molecular sieves and one drop of acetic acid. After 30 minutes, 0.13 mL of a 1M solution of sodium cyanoborohydride in tetrahydrofuran was added and the mixture stirred at room temperature for 18 hours. At this time the reaction mixture was filtered through diatomaceous earth and the filtrate concentrated in vacuo. Purification by flash chromatography on silica gel (chloroform:methanolic ammonium hydroxide, 97:3) gave the title compound, 39 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06147088
출처 데이터셋uspto-grants-2000_11
ORD IDord-4b565d37fcf64e1fbf76b1d070a774de
출처 메모uspto-grants-2000_11