Benzenesulfonamide, 3-amino- → 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide

HRID 79093

反応式

HRID 79093 の反応式
[F:1][C:2]1[CH:21]=[CH:20][C:5]([O:6][C:7]2[CH:15]=[C:14]([C:16]([CH3:19])([CH3:18])[CH3:17])[CH:13]=[CH:12][C:8]=2[C:9]([OH:11])=O)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[NH2:26][C:27]1[CH:28]=[C:29]([S:33]([NH2:36])(=[O:35])=[O:34])[CH:30]=[CH:31][CH:32]=1>C(Cl)Cl.N1C=CC=CC=1.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][C:7]2[CH:15]=[C:14]([C:16]([CH3:17])([CH3:18])[CH3:19])[CH:13]=[CH:12][C:8]=2[C:9]([NH:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([S:33]([NH2:36])(=[O:34])=[O:35])[CH:28]=2)=[O:11])=[CH:20][CH:21]=1

参加物

7

反応物 3

HCID 7377Benzenesulfonamide, 3-amino-HCID 24386Thionyl ChlorideHCID 589880892-(4-Fluorophenoxy)-4-tert-butylbenzoic acid

生成物 1

HCID 248552112-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide収率 50%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 1049Pyridine溶媒HCID 6344Dichloromethane溶媒

実験手順

A solution of 2-(4-fluorophenoxy)-4-tert-butylbenzoic acid (0.11 g, 0.39 mmol) and thionyl chloride (0.28 mL, 3.9 mmol) in CH2Cl2 (10 mL) was stirred at room temperature for 4 h. The solvent was evaporated under reduced pressure, and to the resulting oil was added a solution of 3-amino-benzenesulfonamide (73 mg, 0.42 mmol) in pyridine (4 mL). The solution was stirred at room temperature 15 h. The reaction was diluted with water and extracted with EtOAc. The combined extracts were washed with water, dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by silica gel chromatography (0%-50% EtOAc-hexanes) to obtain a white solid which was recrystallized from EtOAc and hexanes. 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide (85 mg, 50% yield) was obtained as a white solid. LC/MS: m/z 443.3 (M+H)+ at 3.49 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. extractionextracted with EtOAc
  3. washThe combined extracts were washed with water
  4. dry with materialdried over Na2SO4
  5. customevaporated under reduced pressure
  6. customThe residue was purified by silica gel chromatography (0%-50% EtOAc-hexanes)
  7. customto obtain a white solid which
  8. customwas recrystallized from EtOAc and hexanes

出典と根拠

ORDレコード
ord-9f3311df790543d0b65bf661b6c85066
出典データセット
uspto-grants-2014_09
特許番号
US08841483B2

関連ノート

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