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Formaldehyde → 5-[2-(Isopropyloxycarbonylamino)ethylthio]-3-morpholinomethylimidazo[1,2-a]pyridine

HRID 1081757
ノート
印刷プレビュー

反応式

HRID 1081757 の反応式
[CH2:1]=O.[NH:3]1[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[CH:9]([O:12][C:13]([NH:15][CH2:16][CH2:17][S:18][C:19]1[N:24]2[CH:25]=[CH:26][N:27]=[C:23]2[CH:22]=[CH:21][CH:20]=1)=[O:14])([CH3:11])[CH3:10]>C(O)(=O)C>[CH:9]([O:12][C:13]([NH:15][CH2:16][CH2:17][S:18][C:19]1[N:24]2[C:25]([CH2:1][N:3]3[CH2:8][CH2:7][O:6][CH2:5][CH2:4]3)=[CH:26][N:27]=[C:23]2[CH:22]=[CH:21][CH:20]=1)=[O:14])([CH3:11])[CH3:10]
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 712FormaldehydeHCID 8083MorpholineHCID 233628125-[2-(Isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine

生成物 1

HCID 233628355-[2-(Isopropyloxycarbonylamino)ethylthio]-3-morpholinomethylimidazo[1,2-a]pyridine収率 50.1%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

To a solution of an aqueous 37% formalin solution (210 mg, 2.59 mmoles) in acetic acid (2 ml) was added morpholine (226 μl, 2.59 mmoles) under ice-cooling and the mixture was stirred at room temperature for 45 minutes. 5-[2-(isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine (651 mg, 2.33 mmoles) was added, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was diluted with chloroform, washed in turn with aqueous 1N NaOH and saturated saline, and then dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethanol/ethyl acetate=1:10] to obtain 442 mg of the desired product (50.1%, light brown solid).

後処理

  1. temperaturecooling
  2. stirringby stirring at 60° C. for 2 hours
  3. distillationAfter the solvent was distilled off
  4. additionthe residue was diluted with chloroform
  5. washwashed in turn with aqueous 1N NaOH and saturated saline
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationAfter the solvent was distilled off
  8. customthe residue was purified by column chromatography [eluent: ethanol/ethyl acetate=1:10]

出典と根拠

ORDレコード
ord-aceb1454d68d4045a684024308409f1a
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05587383

反応ノート

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