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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1926329생성일: 2026년 10월 26일

1,2-Dimethoxyethane → 4-{4-[6-Amino-5-(3-methylbenzofuran-2-yl)-pyridin-3-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1926329

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참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Potassium CarbonateHCID 11430—
반응물4,4,5,5-Tetramethyl-2-(3-methylbenzofuran-2-yl)-1,3,2-dioxaborolaneHCID 59133090—
반응물tert-butyl 4-(4-(6-amino-5-bromopyridin-3-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 67366272—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매dichloropalladium DCMHCID 18456801—
용매WaterHCID 962—
생성물4-{4-[6-Amino-5-(3-methylbenzofuran-2-yl)-pyridin-3-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl esterHCID 67520994—

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온도100 °C

반응 단계

To the DME solution of 3-methyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzofuran (2.3 mL, 0.58 mmol, 2 eq.) from the previous step were added 4-[4-(6-amino-5-bromopyridin-3-yl)-pyrazol-1-yl]piperidine-1-carboxylic acid tert-butyl ester (BB3) (120 mg, 0.29 mmol, 1 eq.), potassium carbonate (120 mg, 0.87 mmol, 3 eq.), water (0.5 mL), and 1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium DCM (10 mg, 0.01 mmol, 0.05 eq.). The mixture was evacuated and filled with nitrogen (3×) and heated in a microwave reactor to 100° C. for 30 min. The crude was passed through Thiol-SPE to remove Pd. The clear solution was purified with the MDPS. 1H NMR (400 MHz, CD3OD): δ=1.48 (s, 9H), 1.96 (dq, J=4.3, 12.3 Hz, 2H), 2.09 (br. s., 2H), 2.35 (s, 3H), 2.96 (br. s., 2H), 4.21 (br. s., 2H), 4.33-4.43 (m, 1H), 7.29 (dt, J=0.8, 7.4 Hz, 1H), 7.34 (dt, J=1.4, 7.2 Hz, 1H), 7.51 (d, J=7.8 Hz, 1H), 7.59-7.65 (m, 1H), 7.82 (s, 1H), 7.85 (d, J=2.3 Hz, 1H), 8.07 (s, 1H), 8.26 (d, J=2.3 Hz, 1H). MS (ES+): m/z=474.38 (100) [MH+]. HPLC: tR=0.94 min (UPLC-ACQUITY, Analytical).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08178668B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-bad2adfddd584cbfb7ba6c046dac4189
출처 메모uspto-grants-2012_05