Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | 1,3,5-Trimethyl-1,3,5-triazacyclohexane | HCID 7952 | — |
| Edukt | 1-Amino-4-methylpiperazine | HCID 81349 | — |
| Edukt | Rifamycin | HCID 6324616 | — |
| Edukt | Rifamycin S | HCID 6436726 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Rifampicin | HCID 135398735 | — |
Reaktionsschritte
7 g. Rifamycin S are dissolved in 25 ml. dimethylformamide, then, while stirring, there are successively added 2.4 g. acetic acid, 0.6 g. paraformaldehyde and 0.85 g. 1,3,5-trimethyl-hexahydro-1,3,5-triazine. The mixture is then kept at 50° C. for 3 hours until the reaction is completed, with the formation of 3-methyl-1,3-oxazino (5,6-c) rifamycin (thin layer chromatography on silica gel 60 F254 - Merck: blue spot at Rf 0.19, eluent chloroform:methanol 9:1 v/v). 3.1 g. 1-amino-4-methylpiperazine are then added and the reaction is continued at 50° C. for about 1 hour until it is completed, as demonstrated by the disappearance of the blue spot in the TLC. After treatment in the usual way, a high yield (7.2 g.) of rifampicin is obtained. It can easily be purified by crystallisation from acetone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04174320 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-720ad38bec7f46d0aac4239ff9d6ccb0 |
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| Quellennotiz | uspto-grants-1979_11 |
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