Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 1-Methylpiperazine | HCID 53167 | — |
| Edukt | 2-(2-Aminoanilino)-5-methylthiophene-3-carbonitrile | HCID 67445262 | — |
| Lösungsmittel | 1-Methylpiperazine hydrochloride | HCID 12196895 | — |
| Produkt | Olanzapine | HCID 135398745 | — |
Reaktionsschritte
2-(2-Aminoanilino)-5-methylthiophene-3-carbonitrile (10.0 g) is taken in N-methyl-piperazine (60 ml) and N-methyl-piperazine hydrochloride (24 gm). The solution is heated at 120° C. until completion of reaction. The reaction mass is cooled and dichloromethane (100 ml) and water is added. The mixture is cooled up to room temperature and dichloromethane layer is separated. 50 ml dichloromethane is evaporated and cyclohexane is added in clear solution. On Cooling the solution, solid is separated out, which is filtered and dried under vacuum to get Olanzapine Form I. (Purity >99.6%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08044196B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-8deccf48941d4bf2a5acbabb0be7147a |
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| Quellennotiz | uspto-grants-2011_10 |
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