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Acetic Anhydride → 1-(4-(6-Methoxybenzo[d]thiazol-2-yl)-3-((pyridin-3-yloxy)methyl)piperazin-1-yl)ethanone dihydrochloride

HRID 549750
ノート
印刷プレビュー

反応式

HRID 549750 の反応式
[C:1](OC(=O)C)(=[O:3])[CH3:2].[ClH:8].[CH3:9][O:10][C:11]1[CH:33]=[CH:32][C:14]2[N:15]=[C:16]([N:18]3[CH2:23][CH2:22][NH:21][CH2:20][CH:19]3[CH2:24][O:25][C:26]3[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=3)[S:17][C:13]=2[CH:12]=1>C1COCC1>[ClH:8].[ClH:8].[CH3:9][O:10][C:11]1[CH:33]=[CH:32][C:14]2[N:15]=[C:16]([N:18]3[CH2:23][CH2:22][N:21]([C:1](=[O:3])[CH3:2])[CH2:20][CH:19]3[CH2:24][O:25][C:26]3[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=3)[S:17][C:13]=2[CH:12]=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

4

反応物 2

HCID 7918Acetic AnhydrideHCID 667971466-Methoxy-2-(2-((pyridin-3-yloxy)methyl)piperazin-1-yl)benzo[d]thiazole hydrochloride

生成物 1

HCID 667974721-(4-(6-Methoxybenzo[d]thiazol-2-yl)-3-((pyridin-3-yloxy)methyl)piperazin-1-yl)ethanone dihydrochloride収率 85%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
70 °C

実験手順

Acetic anhydride (0.100 mL) was added to a solution of 6-methoxy-2-(2-((pyridin-3-yloxy)methyl)piperazin-1-yl)benzo[d]thiazole hydrochloride (73.2 mg, 0.186 mmol) in THF (2 mL), and the mixture was heated to 70° C. for 2 h. Upon cooling to rt, the reaction mixture was concentrated under reduced pressure and purified by HPLC (5 to 50% MeCN/0.1% TFA in H2O/0.1% TFA gradient). The fractions containing the desired product were brought to pH 12 with 1 N NaOH and were extracted with EtOAc (3×). The combined organics were dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was dissolved in MeOH (1 mL) and treated with 4 M HCl in 1,4-dioxane (6 mL). This was concentrated under reduced pressure, yielding 74.3 mg (85%) of the title compound as a white solid. LC-MS: RT=6.10 min, [M+H]+=399.0.

後処理

  1. temperatureUpon cooling to rt
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. custompurified by HPLC (5 to 50% MeCN/0.1% TFA in H2O/0.1% TFA gradient)
  4. additionThe fractions containing the desired product
  5. extractionwere extracted with EtOAc (3×)
  6. dry with materialThe combined organics were dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. dissolutionThe material was dissolved in MeOH (1 mL)
  10. additiontreated with 4 M HCl in 1,4-dioxane (6 mL)
  11. concentrationThis was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-85850dd1e9ad43e9b5b1efe45a92654c
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943622B2

反応ノート

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