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Hydrochloric Acid → 1,3-Dichloro-6,7,8,9,10,12-hexahydroazepino[2,1-b]quinazolin-12-ol

HRID 375622
ノート
印刷プレビュー

反応式

HRID 375622 の反応式
[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]2[C:3]=1[C:4](=[O:18])[N:5]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][C:6]1=[N:7]2.Cl>C(O)(=O)C.[Zn]>[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]2[C:3]=1[CH:4]([OH:18])[N:5]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][C:6]1=[N:7]2
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 2

HCID 313Hydrochloric AcidHCID 10039448HCID 10039448、化合物

生成物 1

HCID 189925491,3-Dichloro-6,7,8,9,10,12-hexahydroazepino[2,1-b]quinazolin-12-ol

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒

実験手順

To a solution of 2 g of 1,3-dichloro-7,8,9,10-tetrahydroazepino[2,1-b]quinazolin-12(6H)-one in 100 mL of glacial acetic acid at 50° C. was added an intimately mixed mixture of 15 g zinc dust and 15 g silica gel (column chromatography grade). To this mechanically stirred suspension was added dropwise concentrated hydrochloric acid, while the progress of the reaction was followed by TLC (20:1 CHCl3 :MeOH, basified aliquots, extracted into chloroform). When the reaction was essentially complete, excess zinc was filtered off (pyrophoric!) the filtrate was concentrated in vacuo, basified, extracted with chloroform, and the crude extract was chromatographed using 20:1 chloroform:methanol as eluent on a silica gel column. The corresponding fractions after concentration in vacuo gave the 1,3-dichloro-6,7,8,9,10,12-hexahydroazepino[2,1-b]quinazolin-12-ol as an off-white crystalline solid.

後処理

  1. extractionwhile the progress of the reaction was followed by TLC (20:1 CHCl3 :MeOH, basified aliquots, extracted into chloroform)
  2. filtrationexcess zinc was filtered off (pyrophoric!) the filtrate
  3. concentrationwas concentrated in vacuo
  4. extractionextracted with chloroform
  5. extractionthe crude extract
  6. customwas chromatographed
  7. concentrationThe corresponding fractions after concentration in vacuo

出典と根拠

ORDレコード
ord-32976f6cca0941faa0a1b0639cd39fd1
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05486512

反応ノート

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