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Hydrochloric Acid → 3-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propanoic acid

HRID 50083
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HRID 50083 반응식
C[O:2][C:3](=[O:15])[CH2:4][CH2:5][N:6]1[CH:14]=[C:12]([CH3:13])[C:10](=[O:11])[NH:9][C:7]1=[O:8].Cl>[OH-].[Na+]>[N:6]1([CH2:5][CH2:4][C:3]([OH:15])=[O:2])[CH:14]=[C:12]([CH3:13])[C:10](=[O:11])[NH:9][C:7]1=[O:8]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 15138291ThyPropOate

생성물 1

HCID 15195633-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propanoic acid수율 71%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

3-(1-Thyminyl)propanoic acid methyl ester (1 g, 0.0047 mol) was suspended in 2 M sodium hydroxide (15 mL), refluxed for 10 minutes. The pH was adjusted to 0.3 with conc. hydrochloric acid. The solution was extracted with ethyl acetate (10×25 mL). The organic phase was extracted with saturated aqueous sodium chloride, dried over magnesium sulfate, and evaporated to dryness in vacuo, to give the title compound as a white solid (0.66 g, 71%). M.p. 118-121° C. Anal. for C8H10N2O4, found (calc.) C: 48.38 (48.49) H: 5.09 (5.09) N: 13.93 (14.14). The compound showed satisfactory 1H and 13C-NMR spectra.

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후처리

  1. temperaturerefluxed for 10 minutes
  2. extractionThe solution was extracted with ethyl acetate (10×25 mL)
  3. extractionThe organic phase was extracted with saturated aqueous sodium chloride
  4. dry with materialdried over magnesium sulfate
  5. customevaporated to dryness in vacuo

출처 및 근거

ORD 기록
ord-9e163ff779d74aa6810f4c0b5e5babcf
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06710164B1

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