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HRID 217847생성일: 2026년 10월 24일

Hydrochloric Acid → 3-tert-butyl-1-(4-(methylsulfonyl)phenyl)-1H-pyrazol-5-amine

https://huagongshe.com/ko/reaction/217847

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
반응물4-(Methylsulfonyl)phenylhydrazine hydrochlorideHCID 2735181—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
용매Sodium HydroxideHCID 14798—
생성물3-tert-butyl-1-(4-(methylsulfonyl)phenyl)-1H-pyrazol-5-amineHCID 59588828—

반응 단계

4-(methylsulfonyl)phenylhydrazine hydrochloride (1.133 g, 5.09 mmol) and 4,4-dimethyl-3-oxopentanenitrile (0.697 g, 5.57 mmol) were weighed into a 100 mL RBF. 0.2 M HCl in EtOH (42 mL) was added and the suspension was heated to reflux for 27 h, during which time all solids gradually dissolved to give a yellow solution. The solution was diluted with 1 M NaOH(aq) (˜16 mL) to pH 12-13, EtOAc (70 mL) was added and the biphasic system was vigorously stirred for 5 min. The organic layer was isolated, dried (MgSO4), filtered and concentrated to give a yellow crystalline solid. Yield: 1.42 g (95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198279B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-4e01d0d226ac4ac28dcd7f14d33611df
출처 메모uspto-grants-2012_06