돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19840생성일: 2026년 10월 24일

Triphenylphosphine → 5-(1-Isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/19840

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-Isopropylpiperidin-4-olHCID 79681—
반응물Ethyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
반응물Di-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
용매TetrahydrofuranHCID 8028—
생성물5-(1-Isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl esterHCID 4418524666.9%

반응 단계

To a cold (0° C.) solution of 5-hydroxyindole-2-carboxylic acid ethyl ester (purchased at Biosynth, ref H-6350, 20 g, 1.0 eq.), 1-isopropylpiperidin-4-ol (intermediate 1, step 1, 16.75 g, 1.2 eq.) and triphenylphosphine (30.68 g, 1.2 eq.) in tetrahydrofuran (500 mL) was slowly added a solution of di-tert-butylazodicarboxylate (26.93 g, 1.2 eq.) in tetrahydrofuran (100 mL). The reaction mixture was stirred at room temperature for 48 h then evaporated to dryness in vacuo and purified on silica, eluting with a gradient of solvent from dichloromethane/ethyl acetate 19:1 to dichloromethane/methanol/ammonium hydroxide 95:5:0.25. One fraction was isolated and dried in vacuo, to yield 21.53 g (66%) of the desired product as white solid. MS (m/e): 331.1 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-75b64925e93947979722ad6a0bb1f118
출처 메모uspto-grants-2010_06