HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023667Generated: October 27, 2026
Potassium Hydroxide → Potassium 4-[{[(4-fluorophenyl)methyl]imino}(hydroxy)methyl]-1-methyl-2-{2-[(5-methyl-1,3,4-oxadiazole-2-carbonyl)amino]propan-2-yl}-6-oxo-1,6-dihydropyrimidin-5-olate
https://huagongshe.com/reaction/1023667
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Raltegravir | HCID 54671008 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Potassium 4-[{[(4-fluorophenyl)methyl]imino}(hydroxy)methyl]-1-methyl-2-{2-[(5-methyl-1,3,4-oxadiazole-2-carbonyl)amino]propan-2-yl}-6-oxo-1,6-dihydropyrimidin-5-olate | HCID 23668479 | — |
Reaction Steps
A vial (20 ml) was charged with Raltegravir free hydroxy (200 mg) slurry in EtOH:H2O (1000:1, 0.2 ml) at room temperature. The slurry was heated to 50° C. A solution of 45% aqueous KOH (0.044 ml) was added at 50° C. to the mixture. The resulting mixture was stirred for 5.5 h at 50° C. To this mixture was added distilled H2O (1.5 ml) dropwise to produce a colorless solution. The solvent was then removed under reduced pressure to provide wet Raltegravir potassium crystalline Form VI. The product was dried in a vacuum oven at 40° C. for 3.5 hours to provide Raltegravir potassium crystalline Form VI.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722722B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-8b662a9313324e57bc606751f3d7be7b |
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| Source note | uspto-grants-2014_05 |
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