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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10407생성일: 2026년 10월 24일

2-Methylpyrrolidine → Racemic 4-{2-[2-(2-methyl-pyrrolidin-1-yl)-ethyl]-benzooxazol-5-yl}benzonitrile

https://huagongshe.com/ko/reaction/10407

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylpyrrolidineHCID 13003—
반응물4-(2-Vinyl-benzooxazol-5-yl)-benzonitrileHCID 21980091—
용매EthanolHCID 702—
생성물Racemic 4-{2-[2-(2-methyl-pyrrolidin-1-yl)-ethyl]-benzooxazol-5-yl}benzonitrileHCID 11174938100%

반응 단계

A solution of 24.6 mg (0.1 mmol) of 4-(2-vinyl-benzooxazol-5-yl)-benzonitrile and 24 mg of racemic 2-methyl-pyrrolidine (Aldrich, CAS #765-38-8) in 0.25 mL of ethanol was stirred at room temperature for 1 hour, then concentrated in vacuo to a glass to give pure product racemic 4-{2-[2-(2-methyl-pyrrolidin-1-yl)-ethyl]-benzooxazol-5-yl}-benzonitrile 33 mg (100%): 1H NMR (300 MHz, CDCl3) δ 7.85 (d, J=1.8 Hz, 1 H), 7.77 (d, J=8.4 Hz, 2 H), 7.70 (d, J=8.4 Hz, 2 H), 7.58 (d, J=7.5 Hz, 1 H), 7.50 (dd, J=7.5, 1.8 Hz), 3.2–3.32 (m, 4 H), 1.44–2.65 (m, 7 H), 1.15 (m, 3 H); Mass spectrum: [M+H]+ 332.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094790B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-066231d855314bf3955d22c323fbe57e
출처 메모uspto-grants-2006_08