Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 66818620 | HCID 66818620 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66817717 | HCID 66817717 | 66.4% |
Reaction Steps
An aqueous hydrogen bromide solution (80 μL) was added to a mixed solution of 3-tert-butyl-5,7-dimethyl-6-{2-[2-(4-methyl-cyclohexyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-ethyl}-1H-quinazoline-2,4-dione (3.3 mg, 3.41 μmol) in acetic acid (80 μL), and the mixture was heated with stirring at 100° C. for one hour. The reaction solution was returned to room temperature and then concentrated under reduced pressure, and the resulting residue was purified by preparative TLC to give 5,7-dimethyl-6-{2-[2-(4-methyl-cyclohexyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-ethyl}-1H-quinazoline-2,4-dione as a pale yellow solid (1.2 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169254B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0ceb11e2fc644c5b9acd6fec32235e4c |
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| Source note | uspto-grants-2015_10 |
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