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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15985생성일: 2026년 10월 23일

Sulfuric Acid → 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline

https://huagongshe.com/ko/reaction/15985

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Sodium HydroxideHCID 14798—
반응물Sodium NitriteHCID 23668193—
반응물6-bromo-N2-(quinolin-6-ylmethyl)pyrazine-2,3-diamineHCID 45789418—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinolineHCID 5477560858.6%

반응 단계

To a 6° C. mixture of 6-bromo-N2-(quinolin-6-ylmethyl)pyrazine-2,3-diamine (16 g, 48 mmol), AcOH (97 mL) and H2O (97 mL) was added NaNO2 (4.0 g, 58 mmol) in H2O (12 mL) dropwise over 15 min. After 1.5 hours, a 1:1 mixture of concentrated sulfuric acid and water (6 mL) was added dropwise. After 1.5 hours, NaNO2 (0.5 g, 7 mmol) in H2O (2 mL) and a 1:1 mixture of concentrated sulfuric acid and water (5 mL) were added. The reaction was allowed to warm to room temperature overnight. The reaction was re-cooled in an ice bath and over a period of 1.5 hours, a 1:1 mixture of concentrated sulfuric acid and water (30 mL) and NaNO2 (1.5 g, 22 mmol) in H2O (5 mL) was added. Aqueous 3.75 M NaOH (210 mL) was added dropwise and the resulting suspension was filtered. The precipitate was washed sequentially with water and ether, then suspended in dichloromethane:ethanol (1:1) and filtered. The filtrate was washed sequentially with 1M aqueous Na2CO3 and brine, dried over Na2SO4, filtered and concentrated by rotary evaporation to afford 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (9.6 g, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732604B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e96081d2cf5c4d08bafa6aac38b756fb
출처 메모uspto-grants-2010_06