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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251360생성일: 2026년 10월 27일

Triethylamine → 5-Amino-1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/251360

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Hydrazino-4-methylbenzoic acid hydrochlorideHCID 56777508—
반응물Ethyl(ethoxymethylene)cyanoacrylateHCID 86652221—
용매EthanolHCID 702—
생성물5-Amino-1-(5-carboxy-2-methyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 5808900268%

반응 조건

온도65 °C

반응 단계

To a stirred solution of 3-hydrazino-4-methylbenzoic acid hydrochloride (Example 3A, 478 mg, 2.36 mmol, 1.0 eq) in 20 mL of ethanol were added ethyl(ethoxymethylene)cyanoacrylate (399 mg, 2.36 mmol, 1.0 eq) and triethylamine (329 μL, 2.36 mmol, 1.0 eq) and the mixture was heated at 65° C. for 5 hrs. After standing at room temperature overnight, additional 3-hydrazino-4-methylbenzoic acid hydrochloride (159 mg, 0.78 mmol, 0.3 eq) and triethylamine (110 μL, 0.78 mmol, 0.3 eq) and heated for 2.5. The mixture was cooled to room temperature and concentrated. The crude residue was purified by flash chromatography on silica gel (gradient elution from 7/3 hexanes/EtOAc to 1/1 to elute byproducts followed by EtOAc and 9/1 EtOAc/MeOH to elute product) to provide the product as a brown solid (464 mg, 68%). HPLC (4 minute 10-95 gradient) tR 1.87 min; MS m/z 290.1 [M+H]+; 1H NMR (CD3OD), δ 8.08 (d, J=7.0 Hz, 1 H), 7.93 (s, 1 H), 7.76 (s, 1 H), 7.54 (d, J=8.0 Hz, 1 H), 4.29 (q, J=7.1 Hz, 2 H), 2.19 (s, 3 H), 1.35 (d, J=7.1 Hz, 3 H), ppm; 13C NMR (CD3OD), δ 166.5, 163.8, 150.4, 141.7, 139.9, 135.3, 130.8, 129.5, 128.6, 93.8, 58.8, 15.8, 12.9 ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863314B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-65718befb97e478fbdece0aa3ce7c5b2
출처 메모uspto-grants-2011_01