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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872537생성일: 2026년 10월 26일

Hydrochloric Acid → 3-tert-butyl-N-(2-(5-(3-chloro-4-cyano-2-methylphenyl)furan-2-yl)ethyl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/872537

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Amino-2-chloro-3-methylbenzonitrileHCID 21875413—
반응물Sodium NitriteHCID 23668193—
반응물3-tert-butyl-N-(2-(furan-2-yl)-ethyl)-1H-pyrazole-5-carboxamideHCID 178441080—
촉매Ferrous chloride tetrahydrateHCID 16211588—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물3-tert-butyl-N-(2-(5-(3-chloro-4-cyano-2-methylphenyl)furan-2-yl)ethyl)-1H-pyrazole-5-carboxamideHCID 1784219592.6%

반응 조건

온도80 °C

반응 단계

4-amino-2-chloro-3-methylbenzonitrile (0.200 g, 1.20 mmol) was added to a solution of water (2 ml) and conc. HCl (2 ml) and the mixture was stirred vigorously, heated to 80° C. for 15 min and then cooled to −10° C. Sodium nitrite (0.091 g, 1.32 mmol) was dissolved in 0.5 ml of water and added drop wise to the cooled reaction mixture. After 40 min, the mixture was filtered and 3-tert-butyl-N-(2-(furan-2-yl)-ethyl)-1H-pyrazole-5-carboxamide (0.345 g, 1.32 mmol) dissolved in acetone (3 ml) was added to the filtrate. Then, a solution of iron (II) chloride tetrahydrate in water (3 ml) was added portion wise and the mixture was stirred for 15 h at RT. Water (25 ml) was added to the reaction mixture and extracted three times with EtOAc. The combined organic layers were washed with saturated aqueous NaHCO3 and water and dried with Na2SO4, filtered and evaporated to dryness. CombiFlash purification afforded 0.013 g of the title compound. 1H-NMR (400 MHz; d6-DMSO): δ 1.34 (s, 9H), 3.03 (t, 2H), 3.77 (m, 2H), 6.28 (d, 1H), 6.62 (m, 2H), 7.12 (m, 1H), 7.50 (d, 1H), 7.65 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975254B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-69754be82c7c477e94d23066f3fe62a7
출처 메모uspto-grants-2015_03