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Acetonitrile → HCID 68155976、化合物

HRID 1877798
ノート
印刷プレビュー

反応式

HRID 1877798 の反応式
Cl.Cl.[CH3:3][C:4]([CH3:16])([CH2:9][N:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1)[C:5]([O:7][CH3:8])=[O:6].[Cl:17][C:18]1[CH:19]=[CH:20][C:21]2[N:27]=[C:26](Cl)[C:25]3=[CH:29][C:30]([CH3:32])=[CH:31][N:24]3[CH2:23][C:22]=2[CH:33]=1.C(#N)C.C(=O)([O-])[O-].[K+].[K+]>O>[Cl:17][C:18]1[CH:19]=[CH:20][C:21]2[N:27]=[C:26]([N:13]3[CH2:14][CH2:15][N:10]([CH2:9][C:4]([CH3:16])([CH3:3])[C:5]([O:7][CH3:8])=[O:6])[CH2:11][CH2:12]3)[C:25]3=[CH:29][C:30]([CH3:32])=[CH:31][N:24]3[CH2:23][C:22]=2[CH:33]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6342Acetonitrile2 回HCID 11430Potassium CarbonateHCID 68155933Methyl 2,2-dimethyl-3-(piperazin-1-yl)propanoate dihydrochlorideHCID 68156097HCID 68156097、化合物

生成物 1

HCID 68155976HCID 68155976、化合物収率 58.3%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

反応条件

温度
140 °C

実験手順

Dissolve methyl 2,2-dimethyl-3-(piperazin-1-yl)propanoate dihydrochloride (1.61 g, 5.89 mmoles) in water and load on to two SCX-2 (10 g) cartridges. Wash the cartridges with methanol and elute with 2M ammonia in methanol. Concentrate in vacuo, then dissolve the resultant oil in acetonitrile (40 mL). Add 7,11-dichloro-2-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepine (1.167 g, 4.4 mmoles) to the acetonitrile solution. Divide the acetonitrile solution and place in to 2 microwave tubes, add potassium carbonate (0.89 g, 6.79 mmoles) to each microwave tube and heat and stir at 140° C. in the microwave for 3.5 hr. Allow the reaction mixture to cool, filter, wash the solid collected on the sinter with acetonitrile then concentrate the filtrate in vacuo, add methanol and then evaporate to dryness. Treat with more methanol and collect the resultant precipitate, wash the precipitate with methanol to give methyl 3-[4-(7-chloro-2-methyl-5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-yl)piperazin-1-yl]-2,2-dimethylpropanoate as a crystalline solid (1.1 g). MS (m/z): 429.18 (M+1).

後処理

  1. washWash the cartridges with methanol
  2. washelute with 2M ammonia in methanol
  3. concentrationConcentrate in vacuo
  4. dissolutiondissolve the resultant oil in acetonitrile (40 mL)
  5. temperatureheat
  6. temperatureto cool
  7. filtrationfilter
  8. washwash the solid
  9. customcollected on the sinter with acetonitrile
  10. concentrationthen concentrate the filtrate in vacuo
  11. additionadd methanol
  12. customevaporate to dryness
  13. additionTreat with more methanol
  14. customcollect the resultant precipitate
  15. washwash the precipitate with methanol

出典と根拠

ORDレコード
ord-b509904b731e44bd9bf83683cab1d429
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08314092B2

反応ノート

読み込み中…

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