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Sulfuric Acid → 8-Ethyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

HRID 1401404
ノート
印刷プレビュー

反応式

HRID 1401404 の反応式
S(=O)(=O)(O)O.Cl.[CH2:7]([C:9]1[CH:14]=[CH:13][C:12]([NH:15]N)=[CH:11][CH:10]=1)[CH3:8].[CH3:17][N:18]1[CH2:23][CH2:22][CH2:21][CH2:20][C:19]1=O>O1CCOCC1>[CH2:7]([C:9]1[CH:14]=[CH:13][C:12]2[NH:15][C:21]3[CH2:22][CH2:23][N:18]([CH3:17])[CH2:19][C:20]=3[C:11]=2[CH:10]=1)[CH3:8]
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 1118Sulfuric AcidHCID 13603N-Methyl-2-piperidoneHCID 27609704-Ethylphenylhydrazine hydrochloride

生成物 1

HCID 594550988-Ethyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Sulfuric acid is added to a solution of 4-ethyl phenyl hydrazine hydrochloride (1 equiv.) in dioxane, and stirred for 5 min. at RT. N-Methyl piperidone (0.76-1.4 equiv.) is added and the mixture is heated at 80° C. for 3 h. After completion, as monitored by TLC, the reaction mixture is concentrated under reduced pressure and basified to pH 10 using 10% aqueous KOH solution, extracted with EtOAc, dried over anhydrous sodium sulfate and concentrated under reduced pressure using rotary evaporator to provide the desired compound.

後処理

  1. temperaturethe mixture is heated at 80° C. for 3 h
  2. concentrationthe reaction mixture is concentrated under reduced pressure and basified to pH 10
  3. extractionextracted with EtOAc
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customevaporator

出典と根拠

ORDレコード
ord-5073ca927a554003a6eaefcbc1bc7329
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08907097B2

反応ノート

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