HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 58266686, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 58266658 | HCID 58266658 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Water ammonium hydroxide | HCID 86589665 | — |
| Product | HCID 58266686 | HCID 58266686 | — |
Reaction Steps
A solution of hydrogen bromide (33%) in acetic acid (1.10 mL, 6.08 mmol) was added to 6-amino-3-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole (80.1 mg, 0.304 mmol) at 0° C. To the resulting suspension was added bromine (18 μL, 0.34 mmol), and then a 1N solution of sodium nitrite in water (0.43 mL, 0.43 mmol), and the mixture was allowed to warm to ambient temperature. After 1 h, the reaction mixture was diluted with concentrated ammonium hydroxide-water (1:1) and DCM, filtered to remove the solid, and the filtrate layers separated. The aqueous phase was extracted into DCM and the combined organic phase was concentrated in vacuo. The residue was purified by flash chromatography (silica, 0-100% ethyl acetate in hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501765B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d63d30e2dabd4add874d8e4ff8c3fd1d |
| Source note | uspto-grants-2013_08 |