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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2085136생성일: 2026년 10월 24일

(S)-(+)-Glycidyl-4-nitrobenzoate → ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylate

https://huagongshe.com/ko/reaction/2085136

반응식

참여 물질

역할이름HCID투입량
반응물(S)-(+)-Glycidyl-4-nitrobenzoateHCID 10868995—
반응물4-(Naphthalen-2-yl)piperidineHCID 22029264—
반응물Ethyl 4-hydroxy-1-(2-methylpropyl)indole-2-carboxylateHCID 22728995—
생성물ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylateHCID 8658564181.7%

반응 단계

By the reactions in the same manner as in Starting Material Synthesis Example 25 using ethyl 4-hydroxy-1-(2-methylpropyl)indole-2-carboxylate (5.0 g) obtained in Starting Material Synthesis Example 12, (S)-glycidyl nosylate (4.5 g) and 4-(naphthalen-2-yl)piperidine (5.3 g), ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylate (7.5 g) was obtained. This was dissolved in ethanol (40 ml) and water (30 ml) and potassium hydroxide (4.0 g) were added. The mixture was refluxed for 2.5 hr. From the obtained reaction mixture, ethanol was evaporated under reduced pressure and 1N aqueous hydrochloric acid solution (30 ml) was added under ice-cooling. The mixture was extracted with chloroform. The obtained organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and isopropyl ether was added to the obtained oil. The obtained crystals were collected by filtration to give the title compound (6.7 g) as pale-yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06720320B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-61ed45dd80374a12806dcb59d0bc4e2d
출처 메모uspto-grants-2004_04