Tetrahydrofuran → N-[1-[(2Z)-2-amino-2-hydroxyiminoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-5-chloro-1H-indole-2-carboxamide

HRID 1376152ノート

反応式

HRID 1376152 の反応式
Cl.[NH2:2][OH:3].C[O-].[Na+].C1COCC1.[Cl:12][C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([C:22]([NH:24][CH:25]1[CH2:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[N:27]([CH2:35][C:36]#[N:37])[C:26]1=[O:38])=[O:23])=[CH:16]2>CO>[NH2:37]/[C:36](=[N:2]\[OH:3])/[CH2:35][N:27]1[C:28]2[C:33](=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:34][CH:25]([NH:24][C:22]([C:17]2[NH:18][C:19]3[C:15]([CH:16]=2)=[CH:14][C:13]([Cl:12])=[CH:21][CH:20]=3)=[O:23])[C:26]1=[O:38]

参加物

6

実験手順

A solution hydroxylamine hydrochloride (147 mg, 2.11 mmol) in MeOH (4 mL) was added to a solution of sodium methoxide in methanol (0.5 M, 4.2 mL, 2.1 mmol) that had been further diluted with methanol (4 mL). After stirring for 10 minutes, THF (4 mL) was added followed by portionwise addition of 5-chloro-N-[1-(cyanomethyl)-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl]-1H-indole-2-carboxamide (Method 11, 400 mg, 1.06 mmol). The reaction mixture was stirred at ambient temperature for 18 h, partitioned between EtOAc (80 mL) and diluted brine (80 mL), filtered and the layers of the filtrate separated. The organic phase was dried (Na2SO4) and the volatiles removed under reduced pressure to give the title material (191 mg, 44%) as a yellow solid.

後処理

  1. stirringThe reaction mixture was stirred at ambient temperature for 18 h
  2. custompartitioned between EtOAc (80 mL) and diluted brine (80 mL)
  3. filtrationfiltered
  4. customthe layers of the filtrate separated
  5. dry with materialThe organic phase was dried (Na2SO4)
  6. customthe volatiles removed under reduced pressure

出典と根拠

ORDレコード
ord-08be3326669a49aba80cfc5f7732c119
出典データセット
uspto-grants-2007_01
特許番号
US07169927B2

反応ノート

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