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HRID 2074458作成日:2026年10月25日

Phosphorus pentachloride → HCID 178466243、化合物

https://huagongshe.com/reaction/2074458

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus pentachlorideHCID 24819—
反応物N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamideHCID 59799754—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒Ammonium HydroxideHCID 14923—
生成物HCID 178466243HCID 178466243—

反応手順

N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamide 41 (590 mg, 1.871 mmol), Phosphorous pentachloride (390 mg, 1.871 mmol) were dissolved in anhydrous chloroform (20 mL) in a small, argon purged flask fitted with an condenser and magnetic stirbar. The solution was heated to reflux in an oil bath for 4 hours and cooled to room temperature overnight. The mixture was diluted with H2O and chloroform and 2M ammonium hydroxide solution added to adjust pH to 9-10. The mixture was transferred to a separatory funnel and the organic layer collected. The aqueous layer was further extracted with chloroform and the combined organic layers were washed with brine, dried over magnesium sulphate, filtered and concentrated to afford crude. The product was purified using dry silica gel column chromatography eluting with 20 mL portions of solvent system (2.5% 2M NH3 in methanol/95% dichloromethane) to afford a yellow residue 42 2-(4-Ethoxy-benzyl)-5-nitro-1H-benzimidazole. 1H NMR (DMSO) δ: 1.30 (t, 3H, J=6.5), 3.87 (q, 2H, J=7.3), 4.11 (s, 2H), 6.88 (d, 2H, J=8.0), 7.25 (d, 2H, J=7.9), 7.65 (d, 1H, J=8.9), 8.07 (d, 1H, J=9.0), 8.36-8.40 (m, 1H); MS (ESI): 298 (MH+, 100%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07919510B2
出典データセットuspto-grants-2011_04
ORD IDord-a2b153bcfa3a4c59a9c0c9974527216f
出典メモuspto-grants-2011_04