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Hydrazine hydrate (1:1) → HCID 68675033、化合物

HRID 2358461
ノート
印刷プレビュー

反応式

HRID 2358461 の反応式
[CH:1]1([CH2:7][N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[Cl:17])[C:10]([C:18]([OH:20])=O)=[CH:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(Cl)(=O)C(Cl)=O.O.[NH2:28][NH2:29]>ClCCl.C(OCC)C>[CH:1]1([CH2:7][N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[Cl:17])[C:10]([C:18]([NH:28][NH2:29])=[O:20])=[CH:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 24654Hydrazine hydrate (1:1)HCID 65578Oxalyl chlorideHCID 686740091-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid

生成物 1

HCID 68675033HCID 68675033、化合物

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6344Dichloromethane溶媒

実験手順

To a suspension of 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid (as prepared in Example 16; (2.0 g, 6.8 mmol) in dichloromethane (60 ml) was added oxalyl chloride (1.2 ml, 14 mmol) and the reaction stirred for 2 h and left to stand overnight. The solvent and excess reagent was removed in vacuo. The resulting residue was dissolved in dichloromethane (10 ml) and added dropwise to a cooled solution (ice/methanol bath) of hydrazine hydrate (1.7 ml, 34 mmol) in diethyl ether (60 ml) over 5 mins. The reaction mixture was then stirred for a further 40 mins before being reduced to half its volume in vacuo and filtered. The filtrate was concentrated further and the resulting precipitate filtered. The precipitates were combined and dried in vacuo to afford 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid hydrazide (2.3 g, 7 mmol).

後処理

  1. customas prepared in Example 16
  2. waitleft
  3. waitto stand overnight
  4. customThe solvent and excess reagent was removed in vacuo
  5. dissolutionThe resulting residue was dissolved in dichloromethane (10 ml)
  6. stirringThe reaction mixture was then stirred for a further 40 mins
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated further
  9. filtrationthe resulting precipitate filtered
  10. customdried in vacuo

出典と根拠

ORDレコード
ord-4b506a30b1644b17aeef5caa0a6afbff
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07763732B2

反応ノート

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