Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 22125005 | HCID 22125005 | — |
| Product | HCID 22125168 | HCID 22125168 | 142.5% |
Reaction Steps
25 mg of 1-[3-(2-aminoethyl)phenyl]-3-(2-bromophenyl)-7-(4-methoxyanilino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one (prepared in Example 59) was treated with 2 ml of 40% aqueous hydrobromic acid and the mixture heated at 150° C. for 2 hours. The mixture was cooled and evaporated. The residue was triturated with hexane to afford 20 mg (80%) of 1-[3-(2-aminoethyl)phenyl]-3-(2-bromophenyl)-7-(4-hydroxyanilino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one hydrobromide as a white solid of melting point 210° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150373 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-fad29b200f544aab8a22ed2ded475165 |
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| Source note | uspto-grants-2000_11 |
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