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HRID 425177作成日:2026年10月26日

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/425177

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2,4-Dimethoxy-benzyl)-4-(3-morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindoleHCID 59263105—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
溶媒Trifluoroacetic acidHCID 6422—
溶媒AnisoleHCID 7519—
生成物4-(3-Morpholin-4-yl-propoxy)-2,3-dihydro-1H-isoindoleHCID 46915186236.9%

反応手順

A solution of 2-(2,4-dimethoxy-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08106057B2
出典データセットuspto-grants-2012_01
ORD IDord-1cb8e22000f943b997563ebfebcae574
出典メモuspto-grants-2012_01