Triethylamine → 5-(Phthalimidomethylthio)imidazo[1,2-a]pyridine

HRID 5449ノート

反応式

HRID 5449 の反応式
[SH:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1.Br[CH2:12][N:13]1[C:17](=[O:18])[C:16]2=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]2[C:14]1=[O:23].C(N(CC)CC)C>C(O)C>[C:14]1(=[O:23])[N:13]([CH2:12][S:1][C:2]2[N:7]3[CH:8]=[CH:9][N:10]=[C:6]3[CH:5]=[CH:4][CH:3]=2)[C:17](=[O:18])[C:16]2=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]12

参加物

5

反応物 3

HCID 8471TriethylamineHCID 792441H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 178418687HCID 178418687、化合物

生成物 1

HCID 233628645-(Phthalimidomethylthio)imidazo[1,2-a]pyridine収率 69.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00 g, 20 mmoles) and N-bromomethylphthalimide (5.28 g, 22 mmoles) in ethanol (200 ml) was added triethylamine (4.2 ml, 30 mmoles) and the mixture was stirred at room temperature for 1 hour. After the solvent was distilled off, chloroform was added to the residue, which was washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off. Then, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 4.29 g of the desired product (69.4%, pale yellow crystals).

後処理

  1. distillationAfter the solvent was distilled off
  2. additionchloroform was added to the residue, which
  3. washwas washed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled off
  6. customThen, the residue was purified by column chromatography (eluent: ethyl acetate)

出典と根拠

ORDレコード
ord-831db6ca9bbd41e0aaa035a1763a8ec1
出典データセット
uspto-grants-1993_09
特許番号
US05244908

反応ノート

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