HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzyl bromide → 3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzyl bromide | HCID 165021 | — |
| Reactant | HCID 178526838 | HCID 178526838 | — |
| Product | 3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-one | HCID 86703125 | — |
Reaction Steps
The title compound was prepared in analogy to the procedure described for step W2 but using 3-chloro-2-hydroxy-5-nitropyridine and 4-methoxybenzyl bromide. The reaction was quenched with a saturated aqueous solution of sodium bicarbonate. The residue was purified by trituration in EtOAc. tR: 0.98 min (LC-MS 4); ESI-MS: 295.2 [M+H]+ (LC-MS 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969341B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-412f86190428432b81e7fed2a2c315a7 |
| Source note | uspto-grants-2015_03 |