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HRID 1868499作成日:2026年10月26日

1,4-Dioxane → 1-(4-Chlorophenyl)-1,4-diazepane

https://huagongshe.com/reaction/1868499

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物4-(4-Chloro-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 66968317—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Chlorophenyl)-1,4-diazepaneHCID 2136382048%

反応手順

The crude 4-(4-Chloro-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (3.10 g, 10.0 mmol) was dissolved in methylene chloride (1 mL) and treated with 4 N HCL/dioxane (10 mL, 40 mmol). The solution was stirred at rt for 1 hour. The reaction was concentrated in vacuo. The residue was diluted with saturated aqueous sodium bicarbonate (100 mL) and extracted with ethyl acetate (3×30 mL). The combined organics were washed with brine, dried over MgSO4, and evaporated to yield 1.00 g (48%) of the title compound. 1H-NMR (CDCl3) δ 1.90 (2H, m), 2.23 (1H, brs), 2.83 (2H, m), 3.02 (2H, m), 3.54 (4H, m), 6.58 (2H, d, j=9.3 Hz), 7.13 (2H, d, j=9.3 Hz). ESI-MS m/z: 211 (M+1), FAS method rt: 1.04 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07635698B2
出典データセットuspto-grants-2009_12
ORD IDord-840ee8894f4d41659307032a88a2c5ad
出典メモuspto-grants-2009_12