HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Bromothieno[3,2-C]pyridin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Cyanomethyl)thiophene-3-carbonitrile | HCID 22503439 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Bromothieno[3,2-C]pyridin-6-amine | HCID 22503423 | 70% |
Reaction Steps
2-Cyanomethyl-3-cyanothiophene (823 mg) was added to a solution (30 ml) of 25% hydrogen bromide in acetic acid, and the resulting mixture was stirred under ice-cooling for 90 min, which was neutralized with a 8N-aqueous solution of sodium hydroxide and then extracted with ethyl acetate. The organic layer was washed with water, dried (over MgSO4) and evaporated. The residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a yellow solid (894 mg, yield; 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-ed43612da5b14cde9caf1b664ee6cd6d |
| Source note | uspto-grants-2004_09 |