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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18341생성일: 2026년 10월 23일

(1-Benzofuran-2-ylmethyl)(methyl)amine → (E)-N-(benzofuran-2-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamide

https://huagongshe.com/ko/reaction/18341

반응식

참여 물질

역할이름HCID투입량
반응물(1-Benzofuran-2-ylmethyl)(methyl)amineHCID 5048607—
반응물N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amineHCID 10954023—
반응물(e)-3-(2-Oxo-2,3-dihydro-1h-indol-5-yl)acrylic acid hydrochloride saltHCID 66905016—
반응물(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid HydrochlorideHCID 66905305—
생성물(E)-N-(benzofuran-2-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamideHCID 1031652790%

반응 단계

According to the procedure of Example 4, except substituting (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic acid hydrochloride salt (1.60 g, 6.3 mmole) for the (E)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl)acrylic acid hydrochloride salt, and substituting 2-(methylaminomethyl)benzofuran (1.20 g, 6.9 mmole) for the 2-methyl-3-(methylaminomethyl)indole, the title compound (2.0 g, 90%) was prepared as a tan solid: MS (ES) m/e 363 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741339B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-10eda3accd644cba80dd14579da39dcf
출처 메모uspto-grants-2010_06