Lithium hydroxide, monohydrate → HCID 68089228、化合物

HRID 1615688ノート

反応式

HRID 1615688 の反応式
[CH3:1][N:2]1[C:14]2[C:5](=[C:6]3[C:11](=[CH:12][CH:13]=2)[N:10]=[CH:9][CH:8]=[CH:7]3)[N:4]=[C:3]1[CH:15]([CH3:21])[CH2:16][C:17]([O:19]C)=[O:18].O.[OH-].[Li+]>C(#N)C.O>[CH3:1][N:2]1[C:14]2[C:5](=[C:6]3[C:11](=[CH:12][CH:13]=2)[N:10]=[CH:9][CH:8]=[CH:7]3)[N:4]=[C:3]1[CH:15]([CH3:21])[CH2:16][C:17]([OH:19])=[O:18]

参加物

5

反応物 2

HCID 168937Lithium hydroxide, monohydrateHCID 68089342HCID 68089342、化合物

生成物 1

HCID 68089228HCID 68089228、化合物収率 90.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6342Acetonitrile溶媒

実験手順

To a solution of methyl 3-(3-methyl-3H-imidazo[4,5-f]quinolin-2-yl)butanoate (560 mg, 1.97 mmol) in acetonitrile (20 mL) and water (8 mL) was added lithium hydroxide hydrate (249 mg, 5.94 mmol). The mixture was stirred at room temperature overnight. The mixture was concentrated to about 8 mL. The pH of the solution was adjusted to ˜4 with 1N HCl aqueous solution. The mixture was concentrated to dryness and to the residue was added 50 mL of DCM/MeOH v/v 10:1. The precipitate was removed by filtration and the filtrate was concentrated to dryness to give the product as a yellow solid (480 mg, 90% yield). ESI MS: m/z 270.1 [M+H]+.

後処理

  1. concentrationThe mixture was concentrated to about 8 mL
  2. concentrationThe mixture was concentrated to dryness and to the residue
  3. additionwas added 50 mL of DCM/MeOH v/v 10:1
  4. customThe precipitate was removed by filtration
  5. concentrationthe filtrate was concentrated to dryness

出典と根拠

ORDレコード
ord-7910eb83d16d4cfdb1e35daf24aeb738
出典データセット
uspto-grants-2014_07
特許番号
US08765760B2

反応ノート

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