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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251333생성일: 2026년 10월 26일

Triethylamine → 3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acid

https://huagongshe.com/reaction/251333

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-hydrazino-N-methoxy-4-methyl-benzamideHCID 11615346—
반응물3-[5-amino-4-(3-iodo-benzoyl)-pyrazol-1-yl]-N-methoxy-4-methyl-benzamideHCID 11784820—
용매EthanolHCID 702—
생성물3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acidHCID 1120943825%

반응 조건

온도65 °C

반응 단계

To a stirred solution of 3-hydrazino-4-methyl-benzoic acid hydrochloride 2 (242 mg, 1.19 mmol, 1.0 eq) in 25 mL of ethanol was added 2-benzoyl-3-phenylamino-acrylonitrile 4 (296 mg, 1.19 mmol, 1.0 eq, preparation: Grothasu, Davis, J. Am. Chem. Soc., 58, 1334 (1936)) and triethylamine (161 μL, 1.19 mmol, 1.0 eq) and the mixture was heated to 65° C. All solids dissolved when temperature reached 65° C. After three hours, LC-MS indicates consumption of the hydrazine. The solids were filtered to provide 3-(5-amino-4-benzoyl-pyrazol-1-yl)-4-methyl-benzoic acid 5 (95 mg, 25%) as a beige solid: HPLC (4 minute gradient) tR 2.10 min;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863314B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-004e36b6428a4fcc9ba5ad06daf0e6a5
출처 메모uspto-grants-2011_01