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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732343생성일: 2026년 10월 25일

2,2,6,6-Tetramethylpiperidine → 2-[2-(S)-[Bis-(2-methylbenzyl)-amino]-3-(3,5-difluorophenyl)-1-(S)-hydroxypropyl]-pyrrole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/732343

반응식

참여 물질

역할이름HCID투입량
반응물2,2,6,6-TetramethylpiperidineHCID 13035—
반응물tert-butyl 1H-pyrrole-1-carboxylateHCID 643494—
반응물2-(S)-[bis-(2-methylbenzyl)-amino]-3-(3,5-difluorophenyl)-propionaldehydeHCID 86614992—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(S)-[Bis-(2-methylbenzyl)-amino]-3-(3,5-difluorophenyl)-1-(S)-hydroxypropyl]-pyrrole-1-carboxylic acid tert-butyl esterHCID 6881465010%

반응 조건

온도-10 °C

반응 단계

Add n-butyllithium (3.30 mL, 8.25 mmol, 2.5 M in hexanes) to a solution of 2,2,6,6-tetramethylpiperidine (1.40 mL, 8.18 mmol) in tetrahydrofuran (THF) (30 mL) at −78° C. over 2 min. Stir 5 min, then warm to −10° C. and stir 5 min, then cool to −78° C. Add N-tert-butoxycarbonylpyrrole (1.37 mL, 8.25 mmol) in THF (1.6 mL) over 3 min. Stir 30 min and add 2-(S)-[bis-(2-methylbenzyl)-amino]-3-(3,5-difluorophenyl)-propionaldehyde (2.96 g, 7.44 mmol) in THF (15 mL) over 5 min. Stir 60 min at −78° C., warm to 0° C. and stir 60 min. Cool −78° C. and quench with saturated aqueous ammonium chloride solution. Extract with ethyl acetate, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with hexanes and dichloromethane) to give the title compound as a foam (0.416 g, 10%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585885B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-8e478015b76044cc98413c62c33f9d85
출처 메모uspto-grants-2009_09