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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926117생성일: 2026년 10월 27일

Sodium periodate → 6-(4-Methoxybenzyl)-5-oxo-5,6-dihydropyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine-9-carbaldehyde

https://huagongshe.com/reaction/926117

반응식

참여 물질

역할이름HCID투입량
반응물Sodium periodateHCID 23667635—
반응물6-(4-methoxybenzyl)-9-vinylpyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-oneHCID 86705386—
촉매1-ButanolHCID 263—
촉매Osmium TetroxideHCID 30318—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-(4-Methoxybenzyl)-5-oxo-5,6-dihydropyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine-9-carbaldehydeHCID 86705391103.5%

반응 단계

6-(4-Methoxybenzyl)-9-vinylpyrido[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-one (Example 30, 3.96 g, 11.9 mmol) was suspended in THF (80 mL) and heated with a heat gun to effect dissolution. Similarly, sodium periodate (5.84 g, 27.3 mmol) was heated in water (40 mL) to effect dissolution. The above solutions were combined with vigorous stirring. While the stirred mixture was still at 40° C., osmium(VIII) oxide in ten-butanol (2.90 mL, 2.5%, 0.30 mmol) was added and the mixture was stirred vigorously for 4 h. The reaction mixture was diluted with water (300 mL) and extracted with EtOAc (3×150 mL) and DCM (3×150 mL). The combined organic layers were dried (MgSO4) and concentrated to afford the title compound (4.13 g, 99%) as a black solid which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 3.77 (s, 3H), 5.80 (s, 2H), 6.83 (d, J=8.66 Hz, 2H), 7.61 (d, J=8.66 Hz, 2H), 8.41 (s, 1H), 9.10 (d, J=2.13 Hz, 1H), 9.26 (d, J=2.13 Hz, 1H), 10.21 (s, 1H). [M+H]=336.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284335B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-0b8ef88e693e469ca7430edbe01e4957
출처 메모uspto-grants-2016_03