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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23985생성일: 2026년 10월 24일

Tributylphosphine → Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoate

https://huagongshe.com/ko/reaction/23985

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Benzyl N-(3-hydroxypropyl)carbamateHCID 562256—
반응물methyl 3-(5-hydroxy-1H-indol-2-yl)propanoateHCID 22570384—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoateHCID 22570338—

반응 단계

1,1′-(Azodicarbonyl)dipiperidine (370 mg, 1.5 mmol) was added to the solution of methyl 3-(5-hydroxyindolyl)propanoate (220 mg, 1.0 mmol), as prepared in step g of Example 5, 3-(benzyloxycarbonylamino)propanol (230 mg, 1.1 mmol) and tri-n-butylphosphine (305 mg, 1.5 mmol) in tetrahydrofuran (20 mL). After stirring at ambient temperature overnight, the reaction mixture was concentrated and the residue was purified by flash column chromatography on silica gel (0-2% ethyl acetate in methylene chloride) to give the title compound as an off white solid (310 mg, 76%). 1H-NMR (400 MHz, CDCl3) δ 7.35 (m, 5H), 7.22 (d, J=8.9 Hz, 1H), 7.09 (d, J=3.1 Hz, 1H), 7.07 (d, J=2.1 Hz, 1H), 6.86 (dd, J=8.8, 2.4 Hz, 1H), 6.38 (d, J=2.9 Hz, 1H), 5.11 (br s, 3H), 4.41 (t, J=6.8 Hz, 2H), 4.07 (t, J=5.9 Hz, 2H), 3.66 (s, 3H), 3.44 (q, J=6.3 Hz, 2H), 2.81 (t, J=6.8 Hz, 2H), 2.02 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855722B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-b7e30da35c9f479082ec3a09dcec3b98
출처 메모uspto-grants-2005_02