Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Reactant | HCID 131722762 | HCID 131722762 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Trimetrexate Ascorbate | HCID 178493113 | 59.3% |
Reaction Steps
This part of the preparation was carried out, as far as possible, under a nitrogen atmosphere. Equivalent quantities of ascorbic acid (0.463 g) and tributylamine (0.487 g) were heated in 20 ml of 200 proof ethanol at 60° C. to give a clear solution. This was cooled to room temperature and a half-equivalent of trimetrexate trifluoroacetate (0.635 g; assumed unsolvated) added and the mixture heated to near reflux to give a clear yellow solution. To the hot solution was added 50 ml of 2-propanol. A light-colored flocculent solid was immediately precipitated. The mixture was heated at 50° C. for 3 minutes, and then allowed to stand in air for about 1.5 hours. The solid was collected, washed with 2:1 2-propanol/ethanol at room temperature, and immediately transferred to a desiccator and dried (diaphragm pump vacuum) over P2O5 to give 0.425 g of the salt as a very pale yellow-green powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258821B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-08e7a5ef0960439182785a734a63ce72 |
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| Source note | uspto-grants-2001_07 |
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