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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761129Generated: November 1, 2026

Tri-o-tolylphosphine → (E)-N-(1,3-Dimethyl-1H-indol-2-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro[1,8]naphthyridin-3-yl)acrylamide

https://huagongshe.com/reaction/1761129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromo-3,4-dihydro-1,8-naphthyridin-2(1H)-oneHCID 11096325—
ReactantN-(1,3-Dimethyl-1H-indol-2-ylmethyl)-N-methylacrylamideHCID 22593810—
Catalystpalladium(II) acetateHCID 167845—
SolventPropionitrileHCID 7854—
Product(E)-N-(1,3-Dimethyl-1H-indol-2-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro[1,8]naphthyridin-3-yl)acrylamideHCID 2365803059.1%

Reaction Steps

To a stirred solution of N-(1,3-dimethyl-1H-indol-2-ylmethyl)N-methylacrylamide (1.7 g, 7 mmole) in propionitrile (50 mL) was added 6-bromo3,4-dihydro-1H-1,8-naphthyridin-2-one (1.16 g, 5.1 mmole), DIEA (1.8 mL, 10.3 mmole), palladium(II) acetate (112 mg, 0.5 mmole), and tri-o-tolylphosphine (304 mg, 1.0 mmole). The reaction was purged with argon and heated at reflux for 16 hr, then was cooled to RT and concentrated under vacuum. Purification by flash chromatography on silica gel (5% methanol/CHCl3), trituration with ethyl acetate, filtration, and drying under vacuum gave the title compound (1.17 g, 59%) as an off-white solid: LCMS (ES) m/e 389.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-7f8a9e5c2c6148c1911c4062c3f529c6
Source noteuspto-grants-2005_01