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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18332Generated: October 26, 2026

Tri-o-tolylphosphine → Indole naphthyridinone 32

https://huagongshe.com/reaction/18332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromo-3,4-dihydro-1,8-naphthyridin-2(1H)-oneHCID 11096325—
ReactantN-methyl-N-(1,2,7-trimethyl-1H-indol-3-ylmethyl)acrylamideHCID 66905360—
Catalystpalladium(II) acetateHCID 167845—
SolventPropionitrileHCID 7854—
ProductIndole naphthyridinone 32HCID 653989925%

Reaction Steps

A mixture of N-methyl-N-(1,2,7-trimethyl-1H-indol-3-ylmethyl)acrylamide (256 mg, 1 mmole) and 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (227 mg, 1 mmole) in propionitrile (20 mL) was treated with DIEA (0.3 mL), Pd(OAc)2 (29 mg, 0.13 mmole), and tri-o-tolylphosphine (50 mg, 0.16 mmole). The reaction was heated at reflux under argon for 10 h, then was cooled to RT and filtered through supercel. The filtrate was concentrated and the residue was purified by flash chromatography on silica gel to afford the title compound (100 mg, 25%) as an off-white solid: MS (ES) m/e 403.2 (M+H)+. Anal. Calcd for C24H26N4O2.2.75H2O: C, 63.77; H, 7.02; N, 12.39. Found: C, 63.81; H, 7.25; N, 11.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741339B2
Source datasetuspto-grants-2010_06
ORD IDord-7521f4df9bb640d88cf03f314724404e
Source noteuspto-grants-2010_06