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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17428생성일: 2026년 10월 23일

Ethyl 4-piperidinecarboxylate → Ethyl 1-(4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazol-2-yl)piperidine-4-carboxylate

https://huagongshe.com/ko/reaction/17428

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-piperidinecarboxylateHCID 70770—
반응물DiisopropylethylamineHCID 81531—
반응물2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 51041429—
용매DichloromethaneHCID 6344—
생성물Ethyl 1-(4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazol-2-yl)piperidine-4-carboxylateHCID 6858480394.7%

반응 단계

2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-130) (0.20 g, 0.70 mmol) was dissolved in dichloromethane (10 ml), then ethyl isonipecotate (0.12 ml, 0.78 mmol) and diisopropylethylamine (0.15 ml, 0.88 mmol) were added, followed by heating under reflux for 3 hours. This was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified by silica gel column chromatography (dichloromethane:methanol=100:1) to obtain a yellow oil (0.27 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c621a90cb5f249d28996c6376a931ddc
출처 메모uspto-grants-2010_06