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HRID 13537作成日:2026年10月26日

Morpholine → (4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanone

https://huagongshe.com/reaction/13537

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物Sodium HydroxideHCID 14798—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-(4-Formylbenzoyl)-4-isopropylpiperazineHCID 57478581—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanoneHCID 10042344—

反応手順

To a solution of 4-(4-isopropyl-piperazine-1-carbonyl)-benzaldehyde (4.0 g, 15.38 mmol) in THF (40 mL) was added morpholine (2.9 g, 33.83 mmol), and the resulting mixture was stirred at room temperature for 1 h before it was cooled to 0° C. with an ice bath. The reaction mixture was then treated with NaBH(OAc)3 (4.56 g, 21.53 mmol) in portions over 15 min. The resulting suspension was stirred at room temperature until it was deemed complete by HPLC. After completion, 10% NaOH (25 mL) was added and the reaction was vigorously agitated for 15 min. The phases were separated and the aqueous layer was extracted with THF (20 mL). The organic layers were combined, dried (MgSO4), filtered and concentrated to yield the title compound as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728129B2
出典データセットuspto-grants-2010_06
ORD IDord-578d972b992f4013ac9230ab24fabcf8
出典メモuspto-grants-2010_06