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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 916213생성일: 2026년 10월 24일

Carbon Dioxide → 7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine-3-carboxylic acid

https://huagongshe.com/ko/reaction/916213

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물1,10-PhenanthrolineHCID 1318—
반응물HCID 11360216HCID 11360216—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine-3-carboxylic acidHCID 22136263—

반응 조건

온도-78 °C

반응 단계

3-Bromo-7-(2-chloro-4,6-dimethyl phenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine (1.46 g) and a few crystals of 1,10 phenanthroline were dissolved in 25 mL of dry tetrahydrofuran and chilled to −78° C. under an atmosphere of argon. Then a 2.0 M solution of n-butyllithium in cyclohexane was added dropwise until the dark color of the phenanthroline/organolithium complex persisted. Then an additional 2.05 mL of the n-butyllithium solution was added. After 10 minutes, carbon dioxide, generated from dry ice, was bubbled through the reaction mixture for 5 minutes. After the reaction mixture had been stirred at −78° C. for 5 minutes, the cooling bath was removed and the mixture was allowed to warm for 5 minutes before being quenched by the addition of water. The mixture was combined with ethyl acetate and water, acidified with dilute hydrochloric acid, and the phases separated. The ethyl acetate was dried with magnesium sulfate and concentrated. The residue was chromatographed on silica gel eluting with an acetone/hexane gradient to provide 1.11 g of 7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridine-3-carboxylic acid, mp 247.8-248.3° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07268146B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-38d726860a234b598209de457ed4f2de
출처 메모uspto-grants-2007_09