HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 67055903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 2-((5-bromopyridin-3-yl)methylthio)acetate | HCID 67055984 | — |
| Product | HCID 67055903 | HCID 67055903 | 72% |
Reaction Steps
A solution of methyl 2-((5-bromopyridin-3-yl)methylthio)acetate (1.2 g, 4.5 mmol) in NH3 (2.0 M in MeOH, 40 mL) was heated at 80° C. in a sealed vessel for 2 h. After this time, the reaction mixture was allowed to cool to room temperature and then the solvent was evaporated under reduced pressure. The resulting residue was recrystallized from EtOAc/hexanes to provide 2-((5-bromopyridin-3-yl)methylthio)acetamide (0.8 g, 72% yield). LCMS Method W: retention time 1.08 min; [M+1]=263.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575184B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-22c26c2f30dc461fb5d9c43e80e4ecd6 |
| Source note | uspto-grants-2013_11 |