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Bromine → Tert-butyl {3-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-4-methylphenyl}carbamate

HRID 1800503
ノート
印刷プレビュー

反応式

HRID 1800503 の反応式
[S-:1][C:2]#[N:3].[K+].[NH2:5][C:6]1[CH:7]=[CH:8][C:9]([O:12][C:13]2[CH:14]=[C:15]([NH:20][C:21](=[O:27])[O:22][C:23]([CH3:26])([CH3:25])[CH3:24])[CH:16]=[CH:17][C:18]=2[CH3:19])=[N:10][CH:11]=1.BrBr>C(O)(=O)C>[NH2:3][C:2]1[S:1][C:11]2[C:6]([N:5]=1)=[CH:7][CH:8]=[C:9]([O:12][C:13]1[CH:14]=[C:15]([NH:20][C:21](=[O:27])[O:22][C:23]([CH3:25])([CH3:24])[CH3:26])[CH:16]=[CH:17][C:18]=1[CH3:19])[N:10]=2
参加物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 24408BromineHCID 516872Potassium thiocyanateHCID 86646010Tert-butyl {3-[(5-aminopyridin-2-yl)oxy]-4-methylphenyl}carbamate

生成物 1

HCID 86646011Tert-butyl {3-[(2-amino[1,3]thiazolo[5,4-b]pyridin-5-yl)oxy]-4-methylphenyl}carbamate収率 82.2%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒3 回

実験手順

Potassium thiocyanate (1.23 g, 12.7 mmol) was suspended in acetic acid (25 mL), and the mixture was stirred at room temperature for 10 min. A solution of tert-butyl {3-[(5-aminopyridin-2-yl)oxy]-4-methylphenyl}carbamate (1.00 g, 3.17 mmol) in acetic acid (25 mL) was added to the obtained solution, and the mixture was further stirred at room temperature for 10 min. A solution of bromine (531 mg, 3.32 mmol) in acetic acid (20 mL) was slowly added dropwise to the obtained solution. After the completion of the dropwise addition, the mixture was stirred at room temperature for 22 hr. The yielded yellow insoluble material was filtered off, and washed with acetic acid. The filtrate and the washing fluid were combined, and concentrated under reduced pressure. The obtained residue was dissolved in ethyl acetate (50 mL), and the solution was washed with water (50 mL), 5% aqueous sodium hydrogen carbonate solution (50 mL) and saturated brine (50 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate), and the obtained solution was concentrated under reduced pressure to give the title compound (0.97 g, 82%) as a colorless powder.

後処理

  1. stirringthe mixture was further stirred at room temperature for 10 min
  2. additionAfter the completion of the dropwise addition
  3. stirringthe mixture was stirred at room temperature for 22 hr
  4. filtrationThe yielded yellow insoluble material was filtered off
  5. washwashed with acetic acid
  6. concentrationconcentrated under reduced pressure
  7. dissolutionThe obtained residue was dissolved in ethyl acetate (50 mL)
  8. washthe solution was washed with water (50 mL), 5% aqueous sodium hydrogen carbonate solution (50 mL) and saturated brine (50 mL)
  9. dry with materialdried over anhydrous sodium sulfate
  10. filtrationThe insoluble material was filtered off
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. customThe obtained residue was purified by basic silica gel column chromatography (ethyl acetate)
  13. concentrationthe obtained solution was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-c55fa234039748c887eea7476b3dd7ab
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08344135B2

反応ノート

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