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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2101307생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → 4-(7-(4-Chlorophenyl)-3-oxo-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridin-8-yl)benzaldehyde

https://huagongshe.com/reaction/2101307

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참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물4-Formylphenylboronic AcidHCID 591073—
반응물2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
반응물8-bromo-7-(4-chlorophenyl)-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 57799465—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1-ButanolHCID 263—
생성물4-(7-(4-Chlorophenyl)-3-oxo-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridin-8-yl)benzaldehydeHCID 57799463—

반응 조건

온도110 °C

반응 단계

To a stirring solution of 8-bromo-7-(4-chlorophenyl)-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one (100 mg, 0.21 mmol) in n-butanol (1.6 mL) at room temperature under argon was added 4-formylphenylboronic acid (40.4 mg, 0.27 mmol), Pd2(dba)3 (7.6 mg, 0.008 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (13.6 mg, 0.03 mmol) and K3PO4 (88.1 mg, 0.41 mmol). The resulting suspension was purged of oxygen by bubbling with argon for 15 min, sealed in a vial under argon, heated at 110° C. for 5 h, and then cooled to room temperature. The reaction mixture was diluted with EtOAc and washed once with water. The organic layer was dried (MgSO4), filtered, and concentrated under reduced pressure. The crude product was purified by automated silica gel chromatography (eluted with EtOAc/hexanes). Pooling of the desired fractions provided the title compound as a yellow solid, 38.8 mg, 36%. HPLC/MS: retention time=2.73 min, [M+H]+=509.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572808B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-8db678ef6d00497d87cf047f739f5a63
출처 메모uspto-grants-2009_08