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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616153Generated: November 1, 2026

Acetic Acid → Methyl 2-{2-[(4-methoxyphenyl)amino]ethyl}-1-oxo-1,2-dihydroisoquinoline-7-carboxylate

https://huagongshe.com/reaction/1616153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantP-AnisidineHCID 7732—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 1-oxo-2-(2-oxoethyl)-1,2-dihydroisoquinoline-7-carboxylateHCID 86664205—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 2-{2-[(4-methoxyphenyl)amino]ethyl}-1-oxo-1,2-dihydroisoquinoline-7-carboxylateHCID 6728287283.1%

Reaction Steps

A solution of methyl 1-oxo-2-(2-oxoethyl)-1,2-dihydroisoquinoline-7-carboxylate (0.10 g, 0.41 mmol) and 4-methoxyaniline (65 mg, 0.53 mmol) in methanol (2 mL) was stirred at rt for 30 mins. Then acetic acid (2.3 μL, 0.04 mmol) and sodium cyanoborohydride (64 mg, 1.0 mmol) was added and the reaction mixture was stirred at rt overnight. The mixture was diluted with water and extracted with DCM (2×). The combined organic phases were then washed with water, and brine, dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by flash silica gel chromatography (20% to 70% EtOAc/hexanes) to afford methyl 2-{2-[(4-methoxyphenyl)amino]ethyl}-1-oxo-1,2-dihydroisoquinoline-7-carboxylate (0.12 g, 83%). LC-MS: (FA) ES+ 353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765773B2
Source datasetuspto-grants-2014_07
ORD IDord-af57a4746c3946ecabb98b0a0c0956c1
Source noteuspto-grants-2014_07