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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64310생성일: 2026년 10월 24일

Potassium Carbonate → 1-Benzyl-5'-oxo-2'-(4-phenoxyphenyl)-5',6'-dihydro-4'H-spiro[piperidine-4,7'-pyrazolo[1,5-a]pyrimidine]-3'-carbonitrile

https://huagongshe.com/ko/reaction/64310

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 2-(1-benzylpiperidin-4-ylidene)acetateHCID 10377866—
반응물HCID 178509389HCID 178509389—
용매DimethylformamideHCID 6228—
생성물1-Benzyl-5'-oxo-2'-(4-phenoxyphenyl)-5',6'-dihydro-4'H-spiro[piperidine-4,7'-pyrazolo[1,5-a]pyrimidine]-3'-carbonitrileHCID 13698379354.9%

반응 조건

온도80 °C

반응 단계

A mixture of 5-amino-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile (1.0 g, 3.6 mmol), ethyl 2-(1-benzylpiperidin-4-ylidene)acetate (1.1 g, 4.3 mmol) and K2CO3 (745 mg, 5.4 mmol) in DMF (20 mL) was heated to 80° C. for 16 hr under N2. The reaction was quenched with water (20 mL) and extracted with EA (20 mL×3). The combined organic layers were dried over Na2SO4, concentrated and purified by chromatography column on silica gel using 30% of EA in PE as eluant to give the product (950 mg, 54.9%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 11.92 (s, 1H), 7.84 (d, J=8.8 Hz, 2H), 7.48-7.40 (m, 2H), 7.36-7.29 (m, 4H), 7.27-7.23 (m, 1H), 7.20 (t, J=7.6 Hz, 1H), 7.15-7.07 (m, 4H), 3.55 (s, 2H), 3.01 (s, 2H), 2.81-2.73 (m, 2H), 2.39-2.27 (m, 2H), 2.26-2.16 (m, 2H), 1.83-1.74 (m, 2H). MS (ESI, m/e) [M+1]+ 489.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447106B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-808905ad54ce43d5a58d73a27bf6f506
출처 메모uspto-grants-2016_09