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HRID 416242作成日:2026年10月27日

Dibutyltin dichloride → 3-[(4-Morpholin-4-yl-phenylamino)-methyl]1H-indole-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/416242

反応式

関与物質

役割名称HCID仕込み量
反応物Dibutyltin dichlorideHCID 12688—
反応物PhenylsilaneHCID 12752—
反応物Benzenamine, 4-(4-morpholinyl)-HCID 75655—
反応物methyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
溶媒TetrahydrofuranHCID 8028—
生成物3-[(4-Morpholin-4-yl-phenylamino)-methyl]1H-indole-6-carboxylic acid methyl esterHCID 5893066098%

反応手順

To a solution of 3-formyl-1H-indole-6-carboxylic acid methyl ester (500 mg, 2.46 mmol), 4-morpholinoaniline (482.3 mg, 2.71 mmol) and dibutyltin dichloride (76 mg, 0.25 mmol) in THF was added phenylsilane (334 μl, 2.71 mmol). The mixture was stirred at room temperature overnight under nitrogen, THF was evaporated off the mixture and the residue was purified by flash chromatography (hexane/EtOAc, 20/80) to afford the title compound 123 (881 mg, 98%). 1H-NMR (DMSO) δ: 8.00 (d, J=1.0 Hz, 1H), 7.70 (d, J=8.2 Hz, 1H); 7.58 (dd, J=8.4, 1.6 Hz, 1H); 7.52 (d, J=2.0 Hz, 1H); 6.70 (d, J=9.0 Hz, 2H); 6.59 (d, J=9.0 Hz, 2H); 5.48 (t, J=5.8 Hz, 1H); 4.31 (d, J=5.7 Hz, 2H); 3.83 (s, 3H); 3.68 (t, J=4.7 Hz, 4H); 2.86 (t, J=4.7 Hz, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088805B2
出典データセットuspto-grants-2012_01
ORD IDord-a93867ec299d407ea2aeea786393e51a
出典メモuspto-grants-2012_01