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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365915생성일: 2026년 10월 26일

Triethylamine → 3-(1-Boc-2-(r)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridine

https://huagongshe.com/reaction/365915

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물3-(1-Boc-2-(r)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22961807—
촉매HCID 178418397HCID 178418397—
촉매HCID 178505377HCID 178505377—
용매TolueneHCID 1140—
생성물3-(1-Boc-2-(r)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridineHCID 2296181062.2%

반응 조건

온도100 °C

반응 단계

To a solution of 3-(1-BOC-2-(R)-azetidinylmethoxy)-6-chloro-5-bromopyridine (660 mg, 1.75 mmol) in toluene (20 mL) was added NEt3 (0.7 mL), copper (I) iodine (33 mg), tetrakis(triphenylphosphine)palladium (0) (201 mg) and (trimethylsilyl)acetylene (0.30 mL, 2.10 mmol). The reaction mixture was stirred and heated at 100° C. for 16 h. Solvent was evaporated and the residue was chromatographed (silica gel; hexane/EtoAc, 5:1 to 2:1) to afford an oil (430 mg, 62%): 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 9H), 2.20-2.40 (m, 2H), 3.80-3.92 (m, 2H), 4.10 (m, 1H), 4.30 (m,1H), 4.50 (m, 1H), 7.37 (d, (H, J=3.0 Hz), 8.05 (d, 1H, J=3.0 Hz); MS (CI/NH3) m/z 395 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127386
출처 데이터셋uspto-grants-2000_10
ORD IDord-0d484c2eeb0f41ee9ddffa78538276ef
출처 메모uspto-grants-2000_10