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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644122Generated: November 1, 2026

Isoindoline → N-(4-methoxy-2-methylphenyl)isoindoline-2-carboxamide

https://huagongshe.com/reaction/1644122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoindolineHCID 422478—
Reactant4-Methoxy-2-methylphenyl isocyanateHCID 2734905—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-methoxy-2-methylphenyl)isoindoline-2-carboxamideHCID 57527872104.5%

Reaction Steps

To a solution of isoindoline (576 mg, 4.0 mmol) in dry 1,4-dioxane (20 mL) was added 4-methoxy-2-methylphenyl isocyanate (815 mg, 5.0 mmol) under argon at room temperature. The reaction mixture was then stirred at RT overnight. The solvent was evaporated under reduced pressure, and the residue was purified by chromatography on silica gel (EtOAc/hexanes: 1:1) to give the title compound (1.18 g, 84%) as a white solid. 1H NMR (500 MHz, DMSO-d6): δ 2.19 (s, 3H), 3.72 (s, 3H), 4.73 (s, 4H), 6.72 (dd, J=2.5 Hz, 8.5 Hz, 1H), 6.78 (d, J=2.5 Hz, 1H), 7.17 (d, J=8.5 Hz, 1H), 7.30-7.32 (m, 2H), 7.34-7.36 (m, 2H), 7.74 (s, 1H), 13C NMR (DMSO-d6): δ 18.2, 51.9, 55.1, 110.9, 115.1, 122.8, 127.2, 127.8, 130.6, 135.1, 137.0, 154.9, 156.5; MS (MH+, 283); EA calc'd for C17H18N2O2: C, 72.32; H, 6.43; N, 9.92. Found C, 72.16; H, 6.82; N, 9.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124121B2
Source datasetuspto-grants-2012_02
ORD IDord-a6026a2d6ea84f578c548c6c535da68b
Source noteuspto-grants-2012_02