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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1472566생성일: 2026년 10월 25일

Hydrochloric Acid → 1-ethyl-3-[(methyloxy)methyl]-1H-pyrazol-5-amine

https://huagongshe.com/reaction/1472566

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물EthylhydrazineHCID 29062—
반응물4-Methoxy-3-oxobutanenitrileHCID 23091966—
용매EthanolHCID 702—
생성물1-ethyl-3-[(methyloxy)methyl]-1H-pyrazol-5-amineHCID 5751690855.8%

반응 단계

To a 25 mL round bottom was added 4-(methyloxy)-3-oxobutanenitrile (500 mg, 4.42 mmol), ethyl hydrazine (655 mg, 4.42 mmol), and 2 M HCl (2.210 mL, 4.42 mmol) in ethanol (10 mL). The reaction mixture was stirred at the room temperature overnight. The reaction mixture was then evaporated and pardoned between 20 mL of ethyl acetate and 20 mL of 1 M Na2CO3. The organic layer was washed with brine, filtered and evaporated to obtain 1-ethyl-3-[(methyloxy)methyl]-1H-pyrazol-5-amine (450 mg, 2.465 mmol, 55.8% yield) as a yellow oil. The product was used in the next step without further purification. LCMS (M+H)+=156.1; 1H NMR (400 MHz, DMSO-d6) ppm 1.20 (t, J=7.20 Hz, 3 H) 3.19 (s, 3 H) 3.82 (q, J=7.33 Hz, 2 H) 4.11 (s, 2 H) 5.11 (s, 2 H) 5.22 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012479B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-22609fb4c9de4f44b26f1e8f2304282e
출처 메모uspto-grants-2015_04