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Sodium Hydroxide → 4-Amino-6-chloro-5-fluoro-3-vinylpicolinic acid

HRID 75102
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HRID 75102 반응식
[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([O:12]C)=[O:11])[C:3]=1[CH:14]=[CH2:15].[OH-].[Na+]>CO.CC(C)=O>[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([OH:12])=[O:11])[C:3]=1[CH:14]=[CH2:15]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86668309Methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate

생성물 1

HCID 866683084-Amino-6-chloro-5-fluoro-3-vinylpicolinic acid수율 63.2%

시약·촉매·용매 2

HCID 180Acetone용매HCID 887Methanol용매

실험 절차

To a solution of methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate (0.150 g, 0.650 mmol) in methanol (3.25 mL) and acetone (3.25 mL) was added sodium hydroxide (0.078 g, 1.951 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was concentrated, diluted with ethyl acetate, and washed with 1N HCl. The organic phase was dried over Na2SO4, filtered, concentrated, and dried under high vacuum to afford the title compound (89 mg, 0.411 mmol, 63.2% yield) as a white solid: mp 164-166° C.; 1H NMR (400 MHz, DMSO) δ 13.34 (s, 1H), 6.67 (s, 2H), 6.67 (dd, J=17.7, 11.5 Hz, 3H), 5.53 (dd, J=10.4, 1.2 Hz, 1H), 5.49 (dd, J=16.7, 1.1 Hz, 1H); 19F NMR (376 MHz, DMSO) δ −142.00 (s); ESIMS m/z 215 ([M−H)−].

후처리

  1. concentrationThe mixture was concentrated
  2. additiondiluted with ethyl acetate
  3. washwashed with 1N HCl
  4. dry with materialThe organic phase was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customdried under high vacuum

출처 및 근거

ORD 기록
ord-2cfbd132fc7e4bb98a04802b9befe011
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835409B2

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