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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257155Generated: November 1, 2026

Trifluoroacetic acid → HCID 69296251, compound

https://huagongshe.com/reaction/1257155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69298125HCID 69298125—
SolventDichloromethaneHCID 6344—
ProductHCID 69296251HCID 6929625158.7%

Reaction Steps

TFA (10 mL, 134 mmol) was added to a solution of 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2-chlorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-one (4 g, 9.2 mmol) in DCM (50 mL) and heated to reflux for 3 h. The reaction mixture was concentrated under reduced pressure, dissolved in HCl, washed with EtOAc (3×), neutralized with satd. Na2CO3 and extracted with EtOAc (3×). The combined extracts were washed with brine, dried over Na2SO4, concentrated under reduced pressure and purified by chromatography to give 3-(5-amino-2-chlorophenyl)-1-methyl-7-(methylamino)-1,6-naphthyridin-2(1H)-one (1.7 g, 58% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.36 (s, 1H), 7.63 (s, 1H), 7.06-7.00 (m, 2H), 6.54-6.50 (m, 2H), 6.14 (s, 1H), 5.21 (s, 2H), 3.48 (s, 3H), 2.84 (d, J=4.8 Hz, 3H); MS (ESI) m/z: 314.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461179B1
Source datasetuspto-grants-2013_06
ORD IDord-acf017f956b3484489d811b533dfadf7
Source noteuspto-grants-2013_06