Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 44178075 | HCID 44178075 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86651033 | HCID 86651033 | 92.1% |
Reaction Steps
To a solution of 0.090 g (0.21 mmol) of 9-benzylamino-4-oxo-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-4H-1,4a,7-triaza-benzocycloheptene-7-carboxylic acid ethyl ester dissolved in 3.00 mL of glacial acetic acid was added 0.75 mL (4.28 mmol) of hydrobromic acid (33 wt % solution in glacial acetic acid). The resulting mixture was stirred at 80° C. for 16 hours, cooled and evaporated to dryness. Toluene was added to the residue and evaporated. Ethanol was added to the residue and evaporated. The crude was triturated with diethyl ether and dichloromethane and filtered to afford 0.083 g (76%) of the product as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507476B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-d8a76b89f9e049a0bf9045d6cf5bb8ef |
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| Source note | uspto-grants-2013_08 |
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