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HCID 22405287、化合物 → 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one

HRID 441222
ノート
印刷プレビュー

反応式

HRID 441222 の反応式
C([O:3][C:4]([CH2:6][CH2:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:10]=1[N+:16]([O-])=O)=O)C>CO.C(O)(=O)C.[Fe]>[CH3:15][C:12]1[CH:13]=[CH:14][C:9]2[NH:8][CH2:7][CH2:6][C:4](=[O:3])[NH:16][C:10]=2[CH:11]=1
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 1

HCID 22405287HCID 22405287、化合物

生成物 1

HCID 224052058-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one収率 16%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 176Acetic Acid溶媒HCID 887Methanol溶媒

実験手順

A mixture of N-(2-ethoxycarbonylethyl)-4-methyl-2-nitroaniline (11.25 g) and iron powder (12.45 g) in a mixture of methanol (70 ml) and acetic acid (7 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was filtered through celite and the filtrate was evaporated in vacuo. The residue was dissolved with chloroform (50 ml) and the solution was basified with saturated sodium bicarbonate aqueous solution. The solution was filtered through celite and the organic layer was washed with brine. The solution was dried over magnesium sulfate and the solvent was removed. A mixture of the residue (8.00 g) in a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was basified with concentrated ammonium hydroxide and then the resulting solution was extracted with chloroform. Drying over magnesium sulfate, filtering and the removal of solvents afforded a crude product. The crude product was triturated with diethyl ether - isopropyl ether (1:1) to give 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.26 g) as a brown powder.

後処理

  1. temperaturewas refluxed for 1 hour
  2. filtrationThe mixture was filtered through celite
  3. customthe filtrate was evaporated in vacuo
  4. dissolutionThe residue was dissolved with chloroform (50 ml)
  5. filtrationThe solution was filtered through celite
  6. washthe organic layer was washed with brine
  7. dry with materialThe solution was dried over magnesium sulfate
  8. customthe solvent was removed
  9. additionA mixture of the residue (8.00 g)
  10. additionin a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml)
  11. temperaturewas refluxed for 1 hour
  12. temperaturethe solution was cooled to ambient temperature
  13. extractionthe resulting solution was extracted with chloroform
  14. dry with materialDrying over magnesium sulfate
  15. filtrationfiltering
  16. customthe removal of solvents
  17. customafforded a crude product
  18. customThe crude product was triturated with diethyl ether - isopropyl ether (1:1)

出典と根拠

ORDレコード
ord-879d11ac84554005b8862850a9437b3b
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05521170

反応ノート

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