Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | (3S,11aR)-N-(2,4-difluorobenzyl)-6-methoxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydrooxazolo[3,2-d]pyrido[1,2-a]pyrazine-8-carboxamide | HCID 53469001 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Cabotegravir | HCID 54713659 | — |
Reaction Steps
Alternatively, the demethylation can be carried out with LiBr: (3S,11aR)—N-[(2,4-Difluorophenyl)methyl]-3-methyl-6-(methyloxy)-5,7-dioxo-2,3,5,7,11,11a-hexahydro[1,3]oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide (8.609 g) was dissolved in THF (90 mL) and LiBr (3.942 g) was added. The mixture was heated to reflux for 12 h and quenched with H2SO4 (0.5 M, 94.467 g). The resultant suspension was stirred at 20° C. for 2 h and filtered. The solid product was re-slurried in water-THF (50 mL-50 mL) at 20° C. for 2 h. The product was collected by filtration, rinsed with water-THF (1-1, 30 mL), and dried under vacuum to afford the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120817B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-74a565e545934c38be4ddd1ec4f5cb1b |
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| Source note | uspto-grants-2015_09 |
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