2-Aminothiophenol → 2-(3-(Benzo[d]thiazol-2-yl)phenoxy)-2-methylpropanoic acid

HRID 1748998ノート

反応式

HRID 1748998 の反応式
[CH:1]([C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[O:6][C:7]([CH3:14])([CH3:13])[C:8]([O:10]CC)=[O:9])=O.[NH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[SH:25].[OH-].[Na+]>CO>[S:25]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[N:18]=[C:1]1[C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[O:6][C:7]([CH3:13])([CH3:14])[C:8]([OH:10])=[O:9]

参加物

5

反応物 3

HCID 87132-AminothiophenolHCID 14798Sodium HydroxideHCID 18766496Ethyl 2-(3-formylphenoxy)-2-methylpropanoate

生成物 1

HCID 682792962-(3-(Benzo[d]thiazol-2-yl)phenoxy)-2-methylpropanoic acid収率 67.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In a methanol solvent, a solution including Compound 97b (1.0 eq.) and 2-aminothiophenol (1.0 eq.) was stirred at room temperature for 22 hours. After methanol was evaporated, the residual was purified by silica gel column chromatography using hexane and ethyl acetate (14:1) as a developer. The obtained product was dissolved with 1,4-dioxane, and then, 1 N NaOH (1.5 eq.) was added thereto. The reaction mixture was stirred at room temperature for 17 hours, and 1,4-dioxane was evaporated. The reaction mixture was stirred at room temperature for 17 hours, and 1,4-dioxane was evaporated therefrom. The residual was distributed between ethyl acetate and water, an aqueous layer was acidified with 6 N HCl. The produced precipitate was filtered and washed with water to obtain Compound 120.

後処理

  1. customAfter methanol was evaporated
  2. customthe residual was purified by silica gel column chromatography
  3. dissolutionThe obtained product was dissolved with 1,4-dioxane
  4. stirringThe reaction mixture was stirred at room temperature for 17 hours
  5. custom1,4-dioxane was evaporated
  6. stirringThe reaction mixture was stirred at room temperature for 17 hours
  7. custom1,4-dioxane was evaporated
  8. filtrationThe produced precipitate was filtered
  9. washwashed with water

出典と根拠

ORDレコード
ord-0893179ebb1f423a8084b94bb86faae8
出典データセット
uspto-grants-2015_10
特許番号
US09155690B2

反応ノート

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