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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221983생성일: 2026년 10월 24일

1,2-Dichloroethane → 9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8(7H)-one

https://huagongshe.com/ko/reaction/221983

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물Pyrimidine-2-carboxylic acidHCID 12626245—
반응물5-hydrazino-3-phenyl-1,6-naphthyridine-2(1H)-oneHCID 67076057—
용매Acetic AcidHCID 176—
용매DimethylformamideHCID 6228—
생성물9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8(7H)-oneHCID 136352657—

반응 조건

온도150 °C

반응 단계

To a mixture of 5-hydrazino-3-phenyl-1,6-naphthyridine-2(1H)-one (2-3) (1.4 g, 5.55 mmol), 2-pyrimidinecarboxylic acid (0.69 g, 5.55 mmol), HOBt (0.85 g, 5.55 mmol), and DIPEA (0.97 mL, 5.55 mmol) in DMF (50 mL) was added EDC (1.23 g, 6.66 mmol). After stirring for overnight, AcOH (5 mL) was added, and the mixture was heated under microwave irradiation at 150° C. for 15 minutes. The solvent was removed under reduced pressure, and the residue was diluted with MeOH, and added water. The resulting solid was collected by filtration to give 9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8(7H)-one (2-4) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207169B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-b6e29215f372433f9ed8b85f18948545
출처 메모uspto-grants-2012_06