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Ammonia → 2-Amino-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid[2-(4-fluorophenyl)-2-hydroxy-ethyl]-methyl-amide

HRID 1351283
ノート
印刷プレビュー

反応式

HRID 1351283 の反応式
[NH3:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([OH:27])[CH2:10][N:11]([CH3:26])[S:12]([C:15]2[C:16]3[CH2:24][CH2:23][CH2:22][C:21](=[O:25])[C:17]=3[S:18][C:19]=2Br)(=[O:14])=[O:13])=[CH:5][CH:4]=1.Cl>O>[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([OH:27])[CH2:10][N:11]([CH3:26])[S:12]([C:15]2[C:16]3[CH2:24][CH2:23][CH2:22][C:21](=[O:25])[C:17]=3[S:18][C:19]=2[NH2:1])(=[O:14])=[O:13])=[CH:5][CH:4]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 210985782-Bromo-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-2-hydroxy-ethyl]-methyl-amide

生成物 1

HCID 210985752-Amino-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid[2-(4-fluorophenyl)-2-hydroxy-ethyl]-methyl-amide

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
110 °C

実験手順

A concentrated aqueous ammonia (24 mL) was added to 2-bromo-7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid[2-(4-fluorophenyl)-2-hydroxy-ethyl]-methyl-amide (210 mg). After heating at 110° C. for 4 hours, the reaction solution was poured into water, brought to pH 9 with 5N hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate, the residue resulting from the removal of the solvent by evaporation was purified by silica gel column chromatography (hexane/ethyl acetate), and the title compound (145 mg) was obtained as a colorless film.

後処理

  1. extractionextracted with ethyl acetate
  2. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
  3. customthe residue resulting from the removal of the solvent by evaporation
  4. customwas purified by silica gel column chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-1a6c29fe3b4240619097201759043ec4
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07217723B2

反応ノート

読み込み中…

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