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Ethanol → 2-(3-Fluorophenyl)pyrimidine-5-carboxylic acid

HRID 563866
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HRID 563866 반응식
[F:1][C:2]1[CH:3]=[C:4]([C:8]2[N:13]=[CH:12][C:11]([C:14]([O:16]C)=[O:15])=[CH:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1.O1CCCC1.C(O)C>O>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[N:9]=[CH:10][C:11]([C:14]([OH:16])=[O:15])=[CH:12][N:13]=2)[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 8028TetrahydrofuranHCID 45073367Methyl 2-(3-fluorophenyl)pyrimidine-5-carboxylate

생성물 1

HCID 450733632-(3-Fluorophenyl)pyrimidine-5-carboxylic acid수율 89.5%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a solution of methyl 2-(3-fluorophenyl)pyrimidine-5-carboxylate (45 g, 0.19 ml) in a 1:1 mixture of tetrahydrofuran and ethanol (120 mL) was added Li(OH).H2O (12.2 g, 0.29 mol) dissolved in water (120 mL) and the reaction mixture was stirred at room temperature overnight. The reaction was concentrated under reduced pressure, dissolved in water (500 mL), acidified with 1N aqueous HCl and filtered. The residue was washed with water (100 mL×3) and dried to give 37 g (yield 89.5%) of 2-(3-fluorophenyl)pyrimidine-5-carboxylic acid. 1H NMR (DMSO-d6) 7.49 (m, 1H) 7.67 (m, 1H) 8.18 (m, 1H) 8.34 (m, 1H) 9.34 (s, 2H). LRMS (ES+) M+H 219.

후처리

  1. concentrationThe reaction was concentrated under reduced pressure
  2. dissolutiondissolved in water (500 mL)
  3. filtrationfiltered
  4. washThe residue was washed with water (100 mL×3)
  5. customdried

출처 및 근거

ORD 기록
ord-7fdb16652e9a4b83b2e76518d24f0e66
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08067589B2

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