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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18344생성일: 2026년 10월 23일

(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid → (E)-3-(6-aminopyridin-3-yl)-N-(5-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/ko/reaction/18344

반응식

참여 물질

역할이름HCID투입량
반응물(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
반응물5-fluoro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 22139018—
반응물2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indeneHCID 22139048—
반응물(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid HydrochlorideHCID 66905305—
생성물(E)-3-(6-aminopyridin-3-yl)-N-(5-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 1033720341%

반응 단계

According to the procedure of Example 24, except substituting 5-fluoro-1-methyl-3-(methylaminomethyl)-1H-indole (0.2 g, 1.04 mmole) for the 2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indene, and substituting (E)-3-(6-amino-pyridin-3-yl)acrylic acid (0.17 g, 1.04 mmole) for the (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic acid hydrochloride salt, the title compound (0.14 g, 41%) was prepared as an off-white powder: MS (ES) m/e 339 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741339B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5b22d1fcba864c72b2b5c571d3a625bf
출처 메모uspto-grants-2010_06