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3,3-Dimethylglutaric anhydride → 1-(5-Methoxy-pyrimidin-2-yl)-4,4-dimethyl-piperidine-2,6-dione

HRID 1179677
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인쇄 미리보기

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HRID 1179677 반응식
[CH3:1][O:2][C:3]1[CH:4]=[N:5][C:6]([NH2:9])=[N:7][CH:8]=1.[CH3:10][C:11]1([CH3:19])[CH2:17][C:16](=O)[O:15][C:13](=[O:14])[CH2:12]1>ClCCl>[CH3:1][O:2][C:3]1[CH:4]=[N:5][C:6]([N:9]2[C:13](=[O:14])[CH2:12][C:11]([CH3:19])([CH3:10])[CH2:17][C:16]2=[O:15])=[N:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 778133,3-Dimethylglutaric anhydrideHCID 23052442-Amino-5-methoxypyrimidine

생성물 1

HCID 220478711-(5-Methoxy-pyrimidin-2-yl)-4,4-dimethyl-piperidine-2,6-dione수율 40%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
180 °C

실험 절차

A mixture of 5-methoxy-pyrimidin-2-ylamine (1.00 g, 7.99 mmol) and 3,3-dimethylglutaric anhydride (1.14 g, 7.99 mmol) was heated at 180° C. for 9 hours. After cooling to room temperature the reaction mixture was dissolved in a small amount of dichloromethane and purified by flash column chromatography (SiO2, ethyl acetate:heptane 70:30), yielding the title compound (0.79 g, 40% yield) as a white solid.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureAfter cooling to room temperature the reaction mixture
  2. custompurified by flash column chromatography (SiO2, ethyl acetate:heptane 70:30)

출처 및 근거

ORD 기록
ord-d99074cb703c4775969cfb62efcffcd1
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279470B2

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