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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13537생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/13537

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Sodium HydroxideHCID 14798—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(4-Formylbenzoyl)-4-isopropylpiperazineHCID 57478581—
용매TetrahydrofuranHCID 8028—
생성물(4-Isopropyl-piperazin-1-yl)-(4-morpholin-4-ylmethyl-phenyl)-methanoneHCID 10042344—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728129B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-578d972b992f4013ac9230ab24fabcf8
출처 메모uspto-grants-2010_06