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Acetic Acid → 7-Bromobenzo[b]thiophen-2-amine

HRID 1296779
ノート
印刷プレビュー

反応式

HRID 1296779 の反応式
[Br:1][C:2]1[C:10]2[S:9][C:8](C(O)=O)=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C([N:17](CC)C(C)C)(C)C.P(N=[N+]=[N-])(=O)(OC1C=CC=CC=1)OC1C=CC=CC=1.C(O)(=O)C>CN(C=O)C>[Br:1][C:2]1[C:10]2[S:9][C:8]([NH2:17])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 176Acetic AcidHCID 81531DiisopropylethylamineHCID 123414Diphenylphosphoryl azideHCID 179795837-Bromo-1-benzothiophene-2-carboxylic acid

生成物 1

HCID 121122087-Bromobenzo[b]thiophen-2-amine収率 92%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

156 mg (0.61 mmol) of 7-bromo-1-benzothiophene-2-carboxylic acid are mixed with 156.8 mg (1.21 mmol) of N,N-diisopropylethylamine in 4.0 ml of DMF. At 0° C., 183.7 mg (0.67 mmol) of diphenyl phosphorazidate are added. The reaction mixture is left to stand at 8° C. overnight and then stirred into ice-water. It is neutralized with acetic acid, and the resulting precipitate is filtered off with suction and carefully dried at 40° C. The solid is then suspended in xylene and heated under reflux for 1 h. The solvent is removed under reduced pressure, and the residue is put in water and heated for 3 h. The aqueous phase is extracted several times with ethyl acetate. The organic phase is dried over sodium sulfate and then the solvent is removed under reduced pressure. 128 mg of the title compound are isolated in a purity which is suitable for further reactions. The amine is reacted further without further purification.

後処理

  1. waitThe reaction mixture is left
  2. filtrationthe resulting precipitate is filtered off with suction
  3. customcarefully dried at 40° C
  4. temperatureheated
  5. temperatureunder reflux for 1 h
  6. customThe solvent is removed under reduced pressure
  7. temperatureheated for 3 h
  8. extractionThe aqueous phase is extracted several times with ethyl acetate
  9. dry with materialThe organic phase is dried over sodium sulfate
  10. customthe solvent is removed under reduced pressure

出典と根拠

ORDレコード
ord-512f73a9b84f4a2bbe473c5fce6a09d3
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07247728B2

反応ノート

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