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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63364생성일: 2026년 10월 24일

Ammonia → N-(4-(((4-aminonaphthalen-1-yl)oxy)methyl)pyridin-2-yl)-6-ethylpyrazin-2-amine

https://huagongshe.com/ko/reaction/63364

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sulfuric AcidHCID 1118—
반응물AcetonitrileHCID 6342—
반응물Tert-butyl (4-((2-((6-ethylpyrazin-2-yl)amino)pyridin-4-yl)methoxy)naphthalen-1-yl)carbamateHCID 118317293—
용매WaterHCID 962—
생성물N-(4-(((4-aminonaphthalen-1-yl)oxy)methyl)pyridin-2-yl)-6-ethylpyrazin-2-amineHCID 11830595975%

반응 조건

온도20 °C

반응 단계

Acetonitrile (200 mL) was added to tert-butyl (4-((2-((6-ethylpyrazin-2-yl)amino)pyridin-4-yl)methoxy)naphthalen-1-yl)carbamate (Intermediate D (protected)) (10.5 g) and the heterogeneous mixture was stirred at 20° C. Sulfuric acid (4.5 eq, 5.5 mL) was added over 2 h at 20° C. The heterogeneous mixture was stirred for an additional 2 h at 20° C. Aqueous ammonia (10 eq, 17 mL) was added to the reaction mixture over 15 min and the temperature was kept at 20° C. by cooling. Water (33.4 mL) was added to the heterogeneous mixture over 5 min at 20° C. After stirring for 30 min at 20° C., the mixture was cooled to 5° C. and stirred for an additional 2 h at 5° C. The precipitate was filtered and washed with water (33.4 mL) and 2-propanol (18 mL). The product was dried at 50° C. in vacuo for 24 h to give N-(4-(((4-aminonaphthalen-1-yl)oxy)methyl)pyridin-2-yl)-6-ethylpyrazin-2-amine (6.2 g, 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447076B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-1c0ec419f4984b08b49b9cfe7ad78153
출처 메모uspto-grants-2016_09