돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3656생성일: 2026년 10월 23일

4-Methylmorpholine → N-(2-amino-4,6-dioxo-3,5-dipropylcyclohex-1-enyl)-3-phenylbutyramide

https://huagongshe.com/ko/reaction/3656

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물TetrahydrofuranHCID 8028—
반응물3-Phenylbutyric acidHCID 20724—
반응물Isobutyl chloroformateHCID 62365—
반응물5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedioneHCID 5098605—
용매Diethyl EtherHCID 3283—
생성물N-(2-amino-4,6-dioxo-3,5-dipropylcyclohex-1-enyl)-3-phenylbutyramideHCID 18935170—

반응 조건

온도-20 °C

반응 단계

Dissolve 3-phenylbutyric acid (1.0 g, 6.1 mmol) in tetrahydrofuran (20 ml), treat with N-methylmorpholine (0.67 ml, 6.1 mmol) and cool to -20° C. Add isobutyl chloroformate (0.79 ml, 6.1 mmol) and stir for 20 minutes. Then add 1,3-di-n-propyl-5,6-diaminouracil (1.4 g, 6.1 mmol, in 5 ml dimethylformamide) and stir the reaction at -20° C. for 3 hours. Then dilute the reaction with diethyl ether (400 ml) and separate the layers. Rinse the organic layer with saturated sodium bicarbonate (200 ml), 50% aqueous sodium chloride (2×200 ml), dry over anhydrous magnesium sulfate, filter and concentrate under vacuum to provide N-(2-amino-4,6-dioxo-3,5-dipropylcyclohex-1-enyl)-3-phenylbutyramide (2.23 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734052
출처 데이터셋uspto-grants-1998_03
ORD IDord-a89a3e5e7d9441a2aad27464a69c6f6b
출처 메모uspto-grants-1998_03