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Morpholine → HCID 68688845、化合物

HRID 1593387
ノート
印刷プレビュー

反応式

HRID 1593387 の反応式
Cl[C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=2)[N:3]=1.[NH:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1>C1COCC1>[O:18]1[CH2:19][CH2:20][N:15]([C:2]2[CH:11]=[N:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=3)[N:3]=2)[CH2:16][CH2:17]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 8083MorpholineHCID 2357142-Chloro-6-nitroquinoxaline

生成物 1

HCID 68688845HCID 68688845、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Into 10 ml of THF was dissolved 1.16 g of 2-chloro-6-nitroquinoxaline, and then 20 ml of morpholine was added thereto, followed by heating under refluxing for 30 minutes. Then, the solvent was removed by evaporation. Water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium bicarbonate aqueous solution and saturated saline. After the solvent was removed by evaporation, the residue was crystallized from diethyl ether to obtain 1.5 g of the title compound.

後処理

  1. temperatureby heating
  2. temperatureunder refluxing for 30 minutes
  3. customThen, the solvent was removed by evaporation
  4. additionWater was added to the residue
  5. extractionfollowed by extraction with ethyl acetate
  6. washThe organic layer was washed with a saturated sodium bicarbonate aqueous solution and saturated saline
  7. customAfter the solvent was removed by evaporation
  8. customthe residue was crystallized from diethyl ether

出典と根拠

ORDレコード
ord-d99fce1c8fec4496b1606636e2fc06bc
出典データセット
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07297698B2

反応ノート

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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