HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Mitomycin A → 1,1a,2,8,8a,8b-Hexahydro-8-(hydroxymethyl)-8a-methoxy-5-methyl-6-(2-methylallylamino)-azirino[2',3':3,4]pyrrolo-[1,2-a]indole-4,7-dione carbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Mitomycin A | HCID 19972 | — |
| Edukt | 2-Methylallylamine | HCID 76141 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 1,1a,2,8,8a,8b-Hexahydro-8-(hydroxymethyl)-8a-methoxy-5-methyl-6-(2-methylallylamino)-azirino[2',3':3,4]pyrrolo-[1,2-a]indole-4,7-dione carbamate | HCID 19838052 | 107% |
Reaktionsschritte
A solution of 50 mg mitomycin A (0.138 mmol) in 8 ml. of anhydrous methanol was stirred with 29 mg of 2-methylallylamine. The progress of the reaction was periodically checked by TLC and, after 2 hours, the solvent was removed by evaporation under reduced pressure and the residue was purified by column chromatography using silica-gel as adsorbent and ethyl acetate as the eluant. Recrystallization from a mixture of chloroform and hexane gave 30 mg (55% yield) of the desired product as purple crystals having a melting point of >250° C. (decomposing) and providing the following analysis:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04885304 |
| Quelldatensatz | uspto-grants-1989_12 |
| ORD ID | ord-164a7a821f6048f9b0d26bd2ae410984 |
| Quellennotiz | uspto-grants-1989_12 |