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Methanol → Methyl 2-(4,6-dioxo-2-(piperidin-1-yl)-1,4,5,6-tetrahydropyrimidin-5-yl)pentanoate

HRID 1399763
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반응식

HRID 1399763 반응식
S(Cl)(Cl)=O.[OH:5][C:6]1[C:11]([CH:12]([CH2:16][CH2:17][CH3:18])[C:13]([OH:15])=[O:14])=[C:10]([OH:19])[N:9]=[C:8]([N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[N:7]=1.[CH3:26]O>>[O:5]=[C:6]1[CH:11]([CH:12]([CH2:16][CH2:17][CH3:18])[C:13]([O:15][CH3:26])=[O:14])[C:10](=[O:19])[NH:9][C:8]([N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)=[N:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 178447459HCID 178447459, 화합물

생성물 1

HCID 66955652Methyl 2-(4,6-dioxo-2-(piperidin-1-yl)-1,4,5,6-tetrahydropyrimidin-5-yl)pentanoate

실험 절차

To a solution cold solution of methanol (50 mL) was added thionyl chloride (7.25 mL; 100 mmol) dropwise. The acidic solution was added to a flask containing 2-(4,6-dihydroxy-2-(piperidin-1-yl)pyrimidin-5-yl)pentanoic acid (3.07 g; 10.4 mmol) and the mixture was heated to reflux for 18 h. The reaction mixture was concentrated under reduced pressure and the product was used as such in the next reaction.

후처리

  1. additionThe acidic solution was added to a flask
  • temperaturethe mixture was heated
  • temperatureto reflux for 18 h
  • concentrationThe reaction mixture was concentrated under reduced pressure
  • customsuch in the next reaction
  • 출처 및 근거

    ORD 기록
    ord-52a7b312ae83449a87cb87b3a072ba1b
    출처 데이터셋
    uspto-grants-2014_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08906906B2

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