Iodoethane → HCID 20515328、化合物

HRID 67363

反応式

HRID 67363 の反応式
[Mg].[CH2:2](I)[CH3:3].[CH3:5][N:6]1[C:12](=[O:13])[C:11]2[CH:14]=[CH:15][CH:16]=[CH:17][C:10]=2[N:9]2[CH:18]=[N:19][C:20]([CH:21]=[O:22])=[C:8]2[CH2:7]1>C(I)C.C(OCC)C.O1CCCC1>[OH:22][CH:21]([C:20]1[N:19]=[CH:18][N:9]2[C:10]3[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=3[C:12](=[O:13])[N:6]([CH3:5])[CH2:7][C:8]=12)[CH2:2][CH3:3]

参加物

7

反応物 3

HCID 6340IodoethaneHCID 5462224Magnesium2 回HCID 198330205,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde

生成物 1

HCID 20515328HCID 20515328、化合物

試薬・触媒・溶媒 3

HCID 6340Iodoethane触媒HCID 3283Diethyl Ether溶媒2 回HCID 8028Tetrahydrofuran溶媒

実験手順

1.22 g (50.2 mmol) of magnesium shavings are covered with 60 ml of absolute diethyl ether under an argon atmosphere and treated with 2-3 drops of ethyl iodide. When the Grignard reaction starts, a solution of 4.3 ml (51 mmol) of ethyl iodide in 10 ml of absolute diethyl ether is added dropwise at the boiling point. After the magnesium has dissolved completely, the mixture is treated dropwise with a solution, warmed to 30° C., of 0.65 g (40 mmol) of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde in 200 ml of absolute tetrahydrofuran. The yellow coloured suspension is heated to boiling under reflux for ca 5.5 hours, cooled to room temperature and poured into 600 ml of ice/water. The mixture is filtered over Dicalit while rinsing with tetrahydrofuran. After concentration of the filtrate in vacuo, the residue is taken up in 250 ml of chloroform. The chloroform phase is washed twice with 60 ml of water each time, dried over magnesium sulphate and concentrated. The crude product is chromatographed on silica gel using chloroform/methanol (19:1, vol/vol) for the elution. After recrystallisation from ca 40 ml of ethyl acetate, there is obtained 4,5-dihydro-3-(1-hydroxypropyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 145°-147° C.

後処理

  1. customWhen the Grignard reaction
  2. additionthe mixture is treated dropwise with a solution
  3. temperatureis heated
  4. temperatureunder reflux for ca 5.5 hours
  5. filtrationThe mixture is filtered over Dicalit
  6. washwhile rinsing with tetrahydrofuran
  7. washThe chloroform phase is washed twice with 60 ml of water each time
  8. dry with materialdried over magnesium sulphate
  9. concentrationconcentrated
  10. customThe crude product is chromatographed on silica gel
  11. washfor the elution
  12. customAfter recrystallisation from ca 40 ml of ethyl acetate

出典と根拠

ORDレコード
ord-cc51df7b8f2e4bff9052ea487ac481da
出典データセット
uspto-grants-1982_08
特許番号
US04346031

関連ノート

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