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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1486241생성일: 2026년 10월 27일

Triphenylphosphine → Ethyl 2,5-dimethyl-7-[(2,3,6-trifluorobenzyl)oxy]pyrazolo[1,5-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1486241

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2,3,6-Trifluorobenzyl alcoholHCID 145500—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물HCID 178469270HCID 178469270—
용매TetrahydrofuranHCID 8028—
용매tert-Butyl methyl etherHCID 15413—
생성물Ethyl 2,5-dimethyl-7-[(2,3,6-trifluorobenzyl)oxy]pyrazolo[1,5-a]pyridine-3-carboxylateHCID 11785976360.4%

반응 단계

1.2 g (5.25 mmol) of ethyl 7-hydroxy-2,5-dimethylpyrazolo[1,5-a]pyridine-3-carboxylate from Example 8A were dissolved in 48 ml of THF. 1.7 g (10.50 mmol) of 2,3,6-trifluorobenzyl alcohol and 2.9 g (11.03 mmol) of triphenylphosphine were added. Subsequently, 2.2 ml (11.03 mmol) of diisopropyl (E)-diazene-1,2-dicarboxylate were added to the solution, which was stirred at RT for 1 h. 120 ml of tert-butyl methyl ether were added, then the mixture was stirred briefly, and the solids formed were filtered off and dried under high vacuum. 1.2 g of the target compound were obtained (62% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09422285B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-46521d68c9e846b49e694be7013db26e
출처 메모uspto-grants-2016_08