HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-7-methoxy-2-methylfuro[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methoxy-2-methylfuro[2,3-c]pyridine | HCID 58622466 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-7-methoxy-2-methylfuro[2,3-c]pyridine | HCID 118021480 | 64% |
Reaction Steps
A solution of 7-methoxy-2-methylfuro[2,3-c]pyridine (3.2 g, 19.6 mmol) in ACN (30 mL) was treated with NBS (3.5 g, 19.7 mmol). After the mixture was stirred at rt for 18 h, it was concentrated in vacuo and purified by silica gel chromatography (PE/EA=30:1-5:1) to afford the title compound (3.0 g, 64%) as a yellow solid. LCMS (M+H)+=243.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034900B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-9d9f37484c124535985d503359c7995a |
| Source note | uspto-grants-2015_05 |