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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034946Generated: November 1, 2026

2-Methoxy-6-(tributylstannyl)pyrazine → 6-(6-methoxypyrazin-2-yl)-8-(4-morpholinophenylamino)-2,7-naphthyridin-1(2H)-one

https://huagongshe.com/reaction/1034946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-6-(tributylstannyl)pyrazineHCID 16427103—
Reactant6-chloro-8-(4-morpholinophenylamino)-2,7-naphthyridin-1(2H)-oneHCID 86649544—
SolventDimethylformamideHCID 6228—
Product6-(6-methoxypyrazin-2-yl)-8-(4-morpholinophenylamino)-2,7-naphthyridin-1(2H)-oneHCID 58094118—

Reaction Steps

6-chloro-8-(4-morpholinophenylamino)-2,7-naphthyridin-1(2H)-one (30 mg, 0.084 mmol) was dissolved in DMF (1 mL) in a microwave vial and 2-methoxy-6-(tributylstannyl)pyrazine (40 mg, 0.1 mmol) was added followed by PdCl2dppf (6.1 mg, 0.0084 mmol) at room temperature. The vial was flushed with nitrogen and closed the cap and subjected to microwave irradiation at 135 C for 60 minutes. The reaction mixture was diluted with DMSO and purified by prep HPLC. The compound was isolated as a TFA salt. 1H NMR (400 MHz, DMSO-d6) δ 11.14 (s, 1H), 8.96 (s, 1H), 8.33 (s, 1H), 7.68 (s, 1H), 7.67 (d, 2H, J=8.8 Hz), 7.38 (m, 1H), 6.95 (d, 2H, J=8.8 Hz), 6.57 (d, 1H, J=7.2 Hz), 4.0 (s, 3H), 3.69 (t, 4H, J=4.8 Hz), 3.04 (t, 4H, J=4.8 Hz); MS m/z 431.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546370B2
Source datasetuspto-grants-2013_10
ORD IDord-12bbe4ab827b4a8a904d18d2a773b3d3
Source noteuspto-grants-2013_10