Sodium Carbonate → 2-Hydroxy-N-[5-(1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-yl]-acetamide

HRID 1774785노트

반응식

HRID 1774785 반응식
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]3[CH:13]=[C:14]([NH:18][C:19]([CH2:21][O:22]C(=O)C)=[O:20])[CH:15]=[N:16][CH:17]=3)=[CH:9][CH:10]=2)[CH2:5][CH2:4][C:3]1=[O:26].C([O-])([O-])=O.[Na+].[Na+]>CO>[OH:22][CH2:21][C:19]([NH:18][C:14]1[CH:15]=[N:16][CH:17]=[C:12]([C:8]2[CH:7]=[C:6]3[C:11](=[CH:10][CH:9]=2)[N:2]([CH3:1])[C:3](=[O:26])[CH2:4][CH2:5]3)[CH:13]=1)=[O:20]

참가 물질

4

실험 절차

To a solution of acetic acid [5-(1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-ylcarbamoyl]-methyl ester (example 2, 0.025 g, 0.071 mmol) in MeOH (1 mL) was added a 1M aqueous solution of Na2CO3 (0.354 mL) and the reaction mixture was stirred at room temperature for 1 h. The mixture was evaporated to dryness, the residue dissolved in EtOAc (20 mL) and washed with aq. NaHCO3 (5 mL). The organic layer was separated, dried over Na2SO4, filtered and evaporated to dryness to give the title compound (0.02 g, 91%) as light brown solid. MS: 312.1 (M+H+).

후처리

  1. customThe mixture was evaporated to dryness
  2. dissolutionthe residue dissolved in EtOAc (20 mL)
  3. washwashed with aq. NaHCO3 (5 mL)
  4. customThe organic layer was separated
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-0e25e6bb1de44a0bbb8687d3703e8c37
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09260408B2

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