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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242175생성일: 2026년 10월 26일

Hydrochloric Acid → 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/242175

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물HydrazineHCID 9321—
반응물(4-Methoxyphenyl)hydrazineHCID 77023—
반응물(1-Ethoxyethylidene)malononitrileHCID 79450—
용매EthanolHCID 702—
생성물5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrileHCID 6712004181%

반응 조건

온도105 °C

반응 단계

To a stirred solution of 2-(1-ethoxyethylidene)malononitrile (958 mg, 7.04 mmol) in EtOH (12 mL) was added (4-methoxyphenyl)hydrazine (1.12 g, 8.09 mmol). (Prior to using the hydrazine its HCl salt was washed with NaHCO3/CH2Cl2. The organic phase was concentrated and used directly.) The solution was heated to 105° C. in the microwave for 20 minutes. CH2Cl2 was added and the organic phase was washed with 1 M HCl and the organic extract was washed with aqueous NaHCO3. The solution was dried using a phase separator and concentrated under reduced pressure to give 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (1.30 g, 81%) which was used as such in the next step. The procedure was adapted from J. Med. Chem. 2004, 47, 5894-5911.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653112B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-79fa3684f21848b882e7327d35308177
출처 메모uspto-grants-2014_02