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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603446생성일: 2026년 10월 26일

Triphenylphosphine → ethyl ((1S)-5-{2-[(2,6-dimethyl-3-pyridinyl)oxy]ethoxy}-2,3-dihydro-1H-inden-1-yl)acetate

https://huagongshe.com/reaction/603446

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2,6-Dimethyl-3-pyridinolHCID 70732—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물ethyl [(1S)-5-(2-hydroxyethoxy)-2,3-dihydro-1H-inden-1-yl]acetateHCID 59300449—
용매TetrahydrofuranHCID 8028—
생성물ethyl ((1S)-5-{2-[(2,6-dimethyl-3-pyridinyl)oxy]ethoxy}-2,3-dihydro-1H-inden-1-yl)acetateHCID 5930051684%

반응 단계

To a solution of ethyl [(1S)-5-(2-hydroxyethoxy)-2,3-dihydro-1H-inden-1-yl]acetate (Example 249, 50.0 mg, 0.19 mmol) and 2,6-dimethylpyridin-3-ol (46.6 mg, 0.38 mmol) in THF (1.5 mL) were added PPh3 (99.2 mg, 0.38 mmol) and ADDP (95.5 mg, 0.38 mmol). The reaction mixture was vigorously stirred at rt for 24 h, and then directly applied to a silica gel column for purification (1:1 hexanes/EtOAc) to give the product (58.9 mg, 84%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 1.29 (t, 3H) 1.72-1.81 (m, 1H), 2.36-2.2.44 (m, 2H), 2.45 (s, 3H), 2.47 (s, 3H), 2.73 (dd, 1H) 2.82-2.92 (m, 2H), 3.52-3.56 (m, 1H) 4.19 (q, 2H), 4.26-4.33 (m, 4H), 6.75 (d, 1H), 6.82 (s, 1H) 6.92 (d, 1H), 7.05 (d, 1H), 7.08 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906653B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c4f2660a6f224899a0f40533804a2b6a
출처 메모uspto-grants-2011_03