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HRID 368840作成日:2026年10月26日

Diethyl cyanophosphonate → 2-(Isochroman-1-yl)-1-[4-(4-ethoxyphenyl)piperazin-1-yl]-2-methylpropan-1-one

https://huagongshe.com/reaction/368840

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl cyanophosphonateHCID 76257—
反応物Sodium BicarbonateHCID 516892—
反応物2-(3,4-dihydro-1H-2-benzopyran-1-yl)acetic acidHCID 13308864—
反応物1-(4-Ethoxyphenyl)piperazine dihydrochlorideHCID 23288741—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-(Isochroman-1-yl)-1-[4-(4-ethoxyphenyl)piperazin-1-yl]-2-methylpropan-1-oneHCID 23288899—

反応手順

Triethylamine (0.48 ml) is added to a mixture of (-)-(isochroman-1-yl)acetic acid (LXI, EXAMPLE 45 Step 3, 0.2016 g, 1.05 mmol), DMF (1.1 ml), dichloromethane (1.1 ml), 1-(4-ethoxyphenyl)piperazine dihydrochloride (XXIV, 0.2997 g, 1.07 mmol) and diethyl cyanophosphonate (0.21 ml). After 2 hr, saturated sodium bicarbonate is added and the mixture is stirred for 2 hr and then extracted several times with dichloromethane. The combined organic phases are backwashed with saline, dried over magnesium sulfate, concentrated, and the residue chromatographed on silica gel eluting with methanol/dichloromethane (2/98). The appropriate fractions are pooled and concentrated to give a residue which upon crystallization from ethyl acetate/hexane gives 2-(isochroman-1-yl)-1-[4-(4-ethoxyphenyl)piperazin-1-yl]-2-methylpropan-1-one (LXXXII), MS (m/z) 380; IR (mineral oil) 1620, 1248, 1515, 1107, 1444 and 815 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133446
出典データセットuspto-grants-2000_10
ORD IDord-87945354a09d4397ae73c176c22c5a08
出典メモuspto-grants-2000_10