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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362154Generated: October 26, 2026

(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid → (E)-3-(6-aminopyridin-3-yl)-N-(7-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide

https://huagongshe.com/reaction/1362154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
Reactant2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indeneHCID 22139048—
Reactant7-fluoro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 22139066—
Reactant(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid HydrochlorideHCID 66905305—
Product(E)-3-(6-aminopyridin-3-yl)-N-(7-fluoro-1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 1172468728.4%

Reaction Steps

According to the procedure of Example 24, except substituting 7-fluoro-1-methyl-3-(methylaminomethyl)-1H-indole (0.2 g, 1.04 mmole) for the 2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[α]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 (0.1 g, 27%) was prepared as an off-white powder: MS (ES) m/e 339 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-0d56c7ee29674253ac700cc595b1c96a
Source noteuspto-grants-2011_02