Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Mitomycin A | HCID 19972 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | 1-Methyl-3-pyrrolidinol | HCID 93074 | — |
| Product | HCID 86744840 | HCID 86744840 | 42% |
Reaction Steps
A solution of mitomycin A (100 mg) in 2 ml of 1-methyl-3-pyrrolidinol was stirred at room temperature and under nitrogen for 30 minutes with 500 mg of a 1.6% solution of KOH in 1-methyl-3-pyrrolidinol. The reaction mixture was diluted with ether and then decomposed with dry ice. The ether was removed under reduced pressure and the residue left was isolated twice on silica gel using triethylamine as a solvent in the first isolation and 4% of triethylamine in acetone in the second isolation. In both isolation processes the pink substance was extracted from the silica gel with a mixture of triethylamine-acetone 1:3 or 1:4. The extract was concentrated under reduced pressure to give 50 m (42%) of the title compound, having no definite melting point and providing the following analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05023253 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-c07fbec2e3364f5d933e43021948aa03 |
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| Source note | uspto-grants-1991_06 |
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