HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → (5-Bromo-6-fluoro-pyridin-2-yl)-(4-chloro-benzyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amine | HCID 57619459 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (5-Bromo-6-fluoro-pyridin-2-yl)-(4-chloro-benzyl)-amine | HCID 57619198 | — |
Reaction Steps
To (4-chloro-benzyl)-(6-fluoro-pyridin-2-yl)-amine (536, 1.03 g, 4.35 mmol) in acetonitrile (30.0 mL), under an atmosphere of nitrogen, N-bromosuccinimide (0.820 g, 4.61 mol) was added slowly. After 2 hours, the reaction was poured into a solution of sodium thiosulfate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated and crytstallized with ethyl acetate and hexane to give a white solid (537, 1.10 g, 80.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722702B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-47ade783e5644d8e85cc3ca8d04203b6 |
| Source note | uspto-grants-2014_05 |