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1-Methylpiperazine → 4-Methyl-7-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepine

HRID 978269
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 978269
[CH3:1][C:2]1[CH:3]=[C:4]2[NH:10][C:9](=O)[C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=3[N:6]3[CH2:16][CH2:17][C:18]([CH:19]=1)=[C:5]23.[CH3:20][N:21]1[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]1>[Ti](Cl)(Cl)(Cl)Cl.C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([N:24]3[CH2:25][CH2:26][N:21]([CH3:20])[CH2:22][CH2:23]3)[C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=3[N:6]3[CH2:16][CH2:17][C:18]([CH:19]=1)=[C:5]23
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Komponenten

5

Edukt 2

HCID 531671-MethylpiperazineHCID 138232804-Methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one

Produkt 1

HCID 138232734-Methyl-7-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24193Titanium TetrachlorideKatalysatorHCID 1140Toluene
Lösungsmittel
2×

Versuchsvorschrift

A solution of 4-methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one (3.6 g, 14.3 mmoles), N-methylpiperazine (16 ml) and toluene (350 ml) was heated to 110° C. Titanium tetrachloride (4.3 ml) was added in three portions in two minute intervals. The mixture was heated under reflux for two hours and cooled to room temperature. Toluene (500 ml) and ice-water (500 m) were added. The mixture was stirred for 30 minutes and the insoluble material was removed by filtration. The organic phase was separated. The aqueous phase was extracted with toluene (200 ml). The combined toluene solutions were washed with water (300 ml), brine (2 times, 300 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated. The residue was triturated with ethanol:hexane to a solid. Recrystallization of the solid from chloroform:hexane yielded 2.4 g of product. The mother liquor was concentrated and the residue was purified on a silica gel column (60 g, 230-400 mesh) to give a second crop of 1.3 g of product (77% overall yield). Recrystallization from 2-propanol gave the analytical sample, mp 173°-174° C.

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for two hours
  3. customthe insoluble material was removed by filtration
  4. customThe organic phase was separated
  5. extractionThe aqueous phase was extracted with toluene (200 ml)
  6. washThe combined toluene solutions were washed with water (300 ml), brine (2 times, 300 ml)
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was evaporated
  9. customThe residue was triturated with ethanol
  10. customRecrystallization of the solid from chloroform

Quellen und Nachweise

ORD-Eintrag
ord-c4ca7e912fab465c9accc7bb2c441e50
Quelldatensatz
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04663453

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