Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | HCID 67148233 | HCID 67148233 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 448749 | HCID 448749 | — |
| Product | HCID 67148197 | HCID 67148197 | — |
Reaction Steps
p-Fluorobenzylamine (3 eq.) was added to the methyl 3-hydroxy-4-oxo-10-{[(1R)-1-phenylethyl]amino}-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate (prepared as described in Step 5 or Step 5A) dissolved in methanol. The mixture was stirred at 70° C. overnight, then cooled to room temperature for use directly in Step 7. In an alternative procedure (Step 6A), the solvent was removed and the crude product crystallized from acetonitrile several times to obtain a single diasteroisomer of the title compound as the 4-fluorobenzylammonium salt with d.e.>95%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414045B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-46dda1c810c44ed189e84de56743609f |
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| Source note | uspto-grants-2008_08 |
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