Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 86587852 | HCID 86587852 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86587851 | HCID 86587851 | 74% |
Reaction Steps
A mixture of 2,6-dibromo-4-(2-benzyloxycarbonylethyl)-phenyl acridine-9-carboxylate (191 mg, 0.309 mmol), glacial acetic acid (20 ml) and 48% hydrobromic acid (5 ml) was heated at 100° C. for 3 h and then cooled. The mixture was added to water (100 ml) and extracted with 20% methanol in chloroform (100 ml×4). The organic extracts were combined and evaporated and the residue was suspended in chloroform (50 ml) and neutralised with a slight excess of triethylamine. The mixture was washed with water (70 ml×3), and the organic layer was dried over sodium sulphate and evaporated to dryness. The residue was recrystallised from CHCl3 to give the desired product (115 mg, 74%.), mp 240–2° C. FAB-MS m/z 529 [M+, 75%], 511 [10], 486 [10], 207 [100].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169554B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-a85d76e1da3d4daa90387f11341a2fcb |
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| Source note | uspto-grants-2007_01 |
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