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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539370생성일: 2026년 10월 26일

2-Methyltetrahydrofuran → HCID 57386416, 화합물

https://huagongshe.com/reaction/539370

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참여 물질

역할이름HCID투입량
반응물2-MethyltetrahydrofuranHCID 7301—
반응물Potassium CarbonateHCID 11430—
반응물5-Chloropyridine-3-boronic acidHCID 20111877—
반응물3-(Di-tert-butylphosphonium)propane sulfonateHCID 24949187—
반응물HCID 57386415HCID 57386415—
촉매HCID 178479786HCID 178479786—
생성물HCID 57386416HCID 5738641633.4%

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온도90 °C

반응 단계

Sodium tetrachloropalladate(II) (3.52 mg, 0.01 mmol), 3-(di-tert-butylphosphonium)propane sulfonate (6.43 mg, 0.02 mmol), 5-chloropyridin-3-ylboronic acid (51.6 mg, 0.31 mmol) and 7′-bromo-5-methyl-3′,4′-dihydro-2′H-spiro[imidazole-2,1′-naphthalen]-4-amine (Example 51 Step 4, 70 mg, 0.24 mmol) were added to a vial. 2-Methyl-tetrahydrofuran (1 mL) and K2CO3 (2M aq.) (0.359 mL, 0.72 mmol) were added and the mixture was degassed by bubbling N2 (g). The vial was sealed and heated in a microwave reactor at 90° C. for 30 min. EtOAc (5 mL) and water (5 mL) were added and the phases were separated. The aqueous phase was extracted with EtOAc twice and the combined organic layers were dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography (4 g SiO2, 0-10% MeOH containing 0.1M NH3 in DCM). The fractions containing product were combined and concentrated, yielding the title compound (26 mg, 33% yield). 1H NMR (500 MHz, CD3OD) δ ppm 1.85-1.94 (m, 1 H), 2.01 (ddd, 1 H), 2.08-2.17 (m, 1 H), 2.17-2.27 (m, 1 H), 2.35 (s, 3 H), 3.02 (t, 2 H), 6.84 (d, 1 H), 7.34 (d, 1 H), 7.48 (dd, 1 H), 7.97 (t, 1 H), 8.48 (d, 1 H), 8.57 (d, 1 H); MS (ES+) m/z 325 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865911B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-f21ad1a3f0a04e6e93b1d496692b7c07
출처 메모uspto-grants-2014_10