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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Trimethylsilylacetylene | HCID 66111 | — |
| 반응물 | 3-(1-Boc-2-(r)-azetidinylmethoxy)-5-bromo-6-chloropyridine | HCID 22961807 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 촉매 | HCID 178505377 | HCID 178505377 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-(1-Boc-2-(r)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridine | HCID 22961810 | 62.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06127386 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-0d484c2eeb0f41ee9ddffa78538276ef |
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| 출처 메모 | uspto-grants-2000_10 |
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