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HRID 1826058作成日:2026年10月26日

(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/reaction/1826058

反応式

関与物質

役割名称HCID仕込み量
反応物(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
反応物5-fluoro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 22139018—
反応物2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indeneHCID 22139048—
反応物(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid HydrochlorideHCID 66905305—
生成物(E)-3-(6-aminopyridin-3-yl)-N-(5-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 1033720341%

反応手順

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-aminopyridin-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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07049310B2
出典データセットuspto-grants-2006_05
ORD IDord-8db74a41d46647508ccedbbb9f2f195c
出典メモuspto-grants-2006_05