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HRID 479778作成日:2026年10月26日

Sodium hydride → Diethyl [1-methyl-4-phenyl-5-(4-pyridyl)imidazol-2-yl]methoxylmethylphosphonate

https://huagongshe.com/reaction/479778

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Phosphonic acid, P-(chloromethyl)-, diethyl esterHCID 76633—
反応物2-Hydroxymethyl-1-methyl-4-phenyl-5-(4-pyridyl)imidazoleHCID 18771529—
溶媒DimethylformamideHCID 6228—
溶媒HexamethylphosphoramideHCID 12679—
生成物Diethyl [1-methyl-4-phenyl-5-(4-pyridyl)imidazol-2-yl]methoxylmethylphosphonateHCID 86587538—

反応条件

温度0 °C

反応手順

To a suspension of 80% NaH in mineral oil (0.013 g, 0.452 mmol) in DMF at 0° C. was added 1-methyl-2-hydroxymethyl-4-phenyl-5-[4-pyridinyl]imidazole (0.100 g, 0.377 mmol) in DMF. The resulting bright yellow solution was stirred at 0° C. for 0.5 h when diethyl chloromethylphosphonate (0.070 mL, 0.452 mmol) dissolved in 0.079 mL of HMPA was added. The resulting mixture was stirred at 0° C. for 15 min and then warmed to rt. After 5 h, the solution was partitioned between CH2Cl2 and H2O. The organic extract was washed with aqueous NaCl and dried (MgSO4). The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 50:1 CH2Cl2/MeOH. The title compound was obtained as a light amber oil (0.088 g, 56%): ESMS (mnz): 416 (M++H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06645989B2
出典データセットuspto-grants-2003_11
ORD IDord-6407d6b6c7664229be44fea43f14feee
出典メモuspto-grants-2003_11