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HRID 18352생성일: 2026년 10월 23일

Boronic Acid → (S)-4-(5-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1,3,4-oxadiazol-2-yl)phenylboronic acid

https://huagongshe.com/ko/reaction/18352

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참여 물질

역할이름HCID투입량
반응물Boronic AcidHCID 61668—
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물(S)-tert-butyl 2-(5-(4-iodophenyl)-1,3,4-oxadiazol-2-yl)pyrrolidine-1-carboxylateHCID 59345147—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물(S)-4-(5-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1,3,4-oxadiazol-2-yl)phenylboronic acidHCID 5934515622%

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온도100 °C

반응 단계

A mixture of (S)-tert-butyl 2-(5-(4-iodophenyl)-1,3,4-oxadiazol-2-yl)pyrrolidine-1-carboxylate (24) (0.574 g, 1.30 mmol), bis(pinacolato)diboron (0.665 g, 2.62 mmol), KOAc (0.641 g, 6.53 mmol) and Pd(PPh3)4 (0.076 g, 0.0658 mmol) in dioxane (5 mL) was degassed with a stream of Ar for 15 minutes. The mixture was then heated at 100° C. for 12 hours, cooled to room temperature and poured into ethyl acetate/H2O. The layers were separated, the aqueous phase was re-extracted with ethyl acetate (2×) and the combined organic layers were washed (H2O, brine) and dried (Na2SO4) and filtered. The solvent was removed in vacuo and the residue purified by flash chromatography (hexane:ethyl acetate, 1:1) to give a mixture of the title boronate ester (25) and boronic acid (26). This mixture was repurified by prep HPLC (CH3CN:H2O:TFA) to afford (S)-4-(5-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-1,3,4-oxadiazol-2-yl)phenylboronic acid 26 as a colorless solid (0.101 g, 22%). 1HNMR (400 MHz, DMSO-d6) δ 8.31 (s, br, 2H), 7.94-8.00 (m, 4H), 5.03-5.10 (m, 1H), 3.37-3.42 (m, 2H), 2.31-2.40 (m, 1H), 1.92-2.04 (m, 3H). 1.38 (s, 3H), 1.18 (s, 6H); LCMS: Anal. Calcd. for C17H22BN3O5: 359. found: 360 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741347B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-27303017a5fd476888662ce5af72322c
출처 메모uspto-grants-2010_06