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HRID 523486作成日:2026年10月25日

1-(1-Piperidinylcarbonyl)piperazine → 2-[4-(Piperidine-1-carbonyl)piperazin-1-yl]-5,6,7,8-tetrahydro-3H-quinazolin-4-one

https://huagongshe.com/reaction/523486

反応式

関与物質

役割名称HCID仕込み量
反応物1-(1-Piperidinylcarbonyl)piperazineHCID 1095015—
反応物2-(Methylthio)-5,6,7,8-tetrahydroquinazolin-4(3H)-oneHCID 135435256—
溶媒AcetonitrileHCID 6342—
溶媒Isoamyl AlcoholHCID 31260—
生成物2-[4-(Piperidine-1-carbonyl)piperazin-1-yl]-5,6,7,8-tetrahydro-3H-quinazolin-4-oneHCID 136268342—

反応手順

2-Methylsulfanyl-5,6,7,8-tetrahydro-3H-quinazolin-4-one (100 mg; 0.51 mmol) and piperazin-1-ylpiperidin-1-ylmethanone (100.5 mg; 0.51 mmol) are reacted in isoamyl alcohol (1 ml) in accordance with the procedure for Example 1. After a reaction time of 4 h, piperazin-1-ylpiperidin-1-ylmethanone (50.3 mg; 0.26 mmol) and isoamyl alcohol (0.5 ml) are again added, and the mixture is again irradiated in the microwave for 4 h. The crystals obtained after conventional work-up are dissolved in acetonitrile and water and freeze-dried; yield: 17 mg (9%), crystals;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09339503B2
出典データセットuspto-grants-2016_05
ORD IDord-b6969258110b4179bb87e069ddf3fd81
出典メモuspto-grants-2016_05