HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 18449152, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 14783666 | HCID 14783666 | — |
| Reactant | HCID 15176215 | HCID 15176215 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Solvent | Isopropanol methylene chloride | HCID 21966342 | — |
| Product | HCID 18449152 | HCID 18449152 | — |
Reaction Steps
To a solution of 100 mg of 4,8-dichloro-1-methoxy-[1,2,4]triazolo[4,3-a]quinoxaline and 109 mg of triethylamine in DMF (2.0 mL) was added 86 mg of N1-benzothiazol-2-yl-ethane-1,2-diamine. This solution was stirred at room temperature for 18 hrs. and then diluted with 10% IPA/methylene chloride, and washed with water and brine. The extracts were dried over sodium sulfate, filtered, and concentrated. The residue was separated by silica gel chromatography to provide a yellow solid. This solid was dissolved in a 1:1.5 mixture of 48% HBr/AcOH and refluxed for 2 hrs. The reaction mixture was concentrated and the residue was triturated with IPE to provide the hydrobromide salt of the title compound as a yellow solid. MS (M+H)+=412.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202245B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-76a5a10943574ad09d8cb7b6725006ec |
| Source note | uspto-grants-2007_04 |