Acetic Acid → Aptazapine

HRID 1447399ノート

反応式

HRID 1447399 の反応式
[CH3:1][N:2]1[C:19](=O)[C:18](=O)[N:5]2[C:6]3[CH:17]=[CH:16][CH:15]=[CH:14][C:7]=3[CH2:8][N:9]3[CH:13]=[CH:12][CH:11]=[C:10]3[CH:4]2[CH2:3]1.C(O)(=O)C>O1CCCC1.B#B>[CH3:1][N:2]1[CH2:19][CH2:18][N:5]2[C:6]3[CH:17]=[CH:16][CH:15]=[CH:14][C:7]=3[CH2:8][N:9]3[CH:13]=[CH:12][CH:11]=[C:10]3[CH:4]2[CH2:3]1

参加物

5

反応物 2

HCID 176Acetic AcidHCID 128377152-methyl-3,4-dioxo-1,2,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine

生成物 1

HCID 51355Aptazapine

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 6328200Diboron溶媒

実験手順

To the suspension of 12.8 g of 2-methyl-3,4-dioxo-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine in 460 ml of tetrahydrofuran, 200 ml of 1-molar diborane in tetrahydrofuran are added while stirring and cooling with ice. The mixture is refluxed for one hour, again cooled and combined with 25 ml of acetic acid. It is evaporated, the residue taken up in 50 ml of 30% aqueous sodium hydroxide and the mixture extracted with methylene chloride. The extract is dried, evaporated, the residue dissolved in diethyl ether, the solution filtered and the filtrate evaporated, to yield the 2-methyl-1,3,4,14b-tetrahydro-10H--pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine.

後処理

  1. additionare added
  2. temperaturecooling with ice
  3. temperatureThe mixture is refluxed for one hour
  4. temperatureagain cooled
  5. customIt is evaporated
  6. extractionthe mixture extracted with methylene chloride
  7. customThe extract is dried
  8. customevaporated
  9. dissolutionthe residue dissolved in diethyl ether
  10. filtrationthe solution filtered
  11. customthe filtrate evaporated

出典と根拠

ORDレコード
ord-d76781500de2432aae5c7fd6185775b0
出典データセット
uspto-grants-1982_02
特許番号
US04316900

反応ノート

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