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HCID 178470049、化合物 → Ethyl 2-(5-bromobenzo[D]thiazol-2-YL)acetate

HRID 424941
ノート
印刷プレビュー

反応式

HRID 424941 の反応式
[CH2:1]([O:3][C:4]([C:6]1[S:7][C:8]2[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][C:9]=2[NH:10][C:11]=1O)=[O:5])[CH3:2]>C(O)(=O)C.[Zn]>[CH2:1]([O:3][C:4](=[O:5])[CH2:6][C:11]1[S:7][C:8]2[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][C:9]=2[N:10]=1)[CH3:2]
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

4

反応物 1

HCID 178470049HCID 178470049、化合物

生成物 1

HCID 21041508Ethyl 2-(5-bromobenzo[D]thiazol-2-YL)acetate

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒

反応条件

温度
110 °C

実験手順

A mixture of the crude material from Example 2C (2.7 g, 8.5 mmol) in acetic acid (60 mL) and heated to 110° C. Then Zn (18 equivalents) was added slowly in portions over 30 min to the mixture under nitrogen. After the completion the mixture was cooled to room temperature and the Zn residue was filtered off. The filter cake was washed with MeOH. And the combined filtrate was stripped to dryness. The residue was dissolved in 70 mL of chloroform and washed with water twice. The chloroform solution was dried with anhydrous MgSO4 and concentrated to dryness. The crude product was purified by column chromatography (silica gel, 10% EtOAc/Hexane). Purified yield for the three steps from example 2B-2D was 1.11 g (43.3%).

後処理

  1. temperatureAfter the completion the mixture was cooled to room temperature
  2. filtrationthe Zn residue was filtered off
  3. washThe filter cake was washed with MeOH
  4. dissolutionThe residue was dissolved in 70 mL of chloroform
  5. washwashed with water twice
  6. dry with materialThe chloroform solution was dried with anhydrous MgSO4
  7. concentrationconcentrated to dryness
  8. customThe crude product was purified by column chromatography (silica gel, 10% EtOAc/Hexane)
  9. customPurified
  10. customyield for the three steps from example 2B-2D

出典と根拠

ORDレコード
ord-0c77c925ecbb4075b1c0c6b60347fb41
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08106088B2

反応ノート

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