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HRID 1853294作成日:2026年10月26日

1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 6-methylisoquinoline-3-carboxylate

https://huagongshe.com/reaction/1853294

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物SodiumHCID 5360545—
反応物Methyl 2-acetamido-2-(dimethoxyphosphoryl)acetateHCID 11746707—
反応物4-(Dimethoxymethyl)pyridine-3-carbaldehydeHCID 86673065—
溶媒DichloromethaneHCID 6344—
生成物Methyl 6-methylisoquinoline-3-carboxylateHCID 2224364462.7%

反応条件

温度0 °C

反応手順

To a cold solution of 4-Dimethoxymethyl-pyridine-3-carbaldehyde (tetrahedron letters 2004 (45), 553-556) (400 mg, 1.91 mmol) in dichloromethane (10 ml) was slowly added a solution of Acetylamino-(dimethoxy-phosphoryl)-acetic acid methyl ester (synthesis 1984, 53-60) (503 mg, 2.1 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.31 ml, 2.1 mmol). The solution was stirred at 0° C. for 1 hour then at room temperature for 18 hours. The mixture was poured onto a cold saturated solution of sodium hydrogenocarbonate, extracted with dichloromethane, dried over sodium sulfate and concentrated to dryness. The residue was dissolved in toluene (49 ml) and treated with p-toleunesulfonic acid (315 mg, 1.66 mmol). The mixture was heated at reflux temperature for 18 hours and then concentrated under vacuum. The brown residue was dissolved in ethyl acetate, washed with a saturated solution of sodium hydrogenocarbonate, brine, dried over sodium sulfate and concentrated to yield methyl 6-methyl-isoquinoline-3-carboxylate (241 mg, 62%) as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08962627B2
出典データセットuspto-grants-2015_02
ORD IDord-9472ff5011434884ad2bdd85d6a2b29c
出典メモuspto-grants-2015_02