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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355710Generated: November 2, 2026

2-(2,4-Dimethoxy-benzyl)-4-(3-morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindole → 4-(3-Morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindole

https://huagongshe.com/reaction/2355710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2,4-Dimethoxy-benzyl)-4-(3-morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindoleHCID 59263105—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
Product4-(3-Morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindoleHCID 46915186236.9%

Reaction Steps

A solution of 2-(2,4-dim ethoxy-benzyl)-4-(3-morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindole (233 mg, 0.56 mmol) in trifluoroacetic acid (1.0 mL) and anisole (0.5 mL) was heated at 150° C. under microwave irradiation for 10 minutes. The mixture was diluted with diethyl ether and extracted twice with water. The combined aqueous extracts were concentrated to give an oil which was dissolved in methanol and concentrated in vacuo to afford the title compound as a brown oil (348 mg, including residual TFA and/or water). 1H NMR (methanol-d4) 7.40 (1H, t), 7.03 (1H, d), 6.99 (1H, d), 4.63 (2H, s), 4.59 (2H, s), 4.21 (2H, t), 4.14-4.04 (2H, m), 3.85-3.73 (2H, m), 3.61-3.52 (2H, m), 3.41-3.36 (2H, m), 3.25-3.13 (2H, m), 2.32-2.25 (2H, m). MS: [M+H]+ 263.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754725B2
Source datasetuspto-grants-2010_07
ORD IDord-9cce5e1c7afb4fddaa23c93e9583b57b
Source noteuspto-grants-2010_07