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Hexahydro-1,4-diazepine → 1-pyrimidin-2-yl-1,4-diazepane

HRID 2376653
ノート
印刷プレビュー

反応式

HRID 2376653 の反応式
Cl[C:2]1[N:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[NH:8]1[CH2:14][CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1>CCO>[N:3]1[CH:4]=[CH:5][CH:6]=[N:7][C:2]=1[N:8]1[CH2:14][CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1
参加物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 68163Hexahydro-1,4-diazepineHCID 744042-Chloropyrimidine

生成物 1

HCID 27724091-pyrimidin-2-yl-1,4-diazepane

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

An ice bath is used to cool a solution of 3 g of 2-chloropyrimidine in 20 ml of EtOH which is then admixed dropwise with a solution of 13 g of 1,4-diazepane in 50 ml of EtOH, left with stirring in the cold for 30 minutes and then at AT for 24 hours. It is concentrated under vacuum, the residue is taken up with 100 ml of AcOEt and 100 ml of saturated K2CO3 solution, the system is decanted, the organic phase is diluted by adding 100 ml of AcOEt, the organic phase is washed with saturated K2CO3 solution and dried over Na2SO4 and the solvent is evaporated under vacuum. This gives the expected product, which is used as it is.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customAn ice bath is used
  2. waitleft
  3. waitat AT for 24 hours
  4. concentrationIt is concentrated under vacuum
  5. customthe system is decanted
  6. additionthe organic phase is diluted
  7. additionby adding 100 ml of AcOEt
  8. washthe organic phase is washed with saturated K2CO3 solution
  9. dry with materialdried over Na2SO4
  10. customthe solvent is evaporated under vacuum

出典と根拠

ORDレコード
ord-bcba9d8cec114a779f4dd6f0b92c6384
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07468368B2

反応ノート

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