Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 67154999 | HCID 67154999 | — |
| Product | HCID 86674841 | HCID 86674841 | — |
Reaction Steps
HBr (3.84 mL, 34.0 mmol) was added to 6-chloro-2-(4-diethoxymethyl-pyridin-3-yl)-1-methyl-1H-benzoimidazole (0.470 g, 1.359 mmol), and the reaction mixture was stirred for 10 min. The reaction was cooled to 0° C. and quenched with saturated aqueous sodium bicarbonate solution. It was extracted with DCM twice. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford 3-(6-chloro-1-methyl-1H-benzoimidazol-2-yl)-pyridine-4-carbaldehyde. MS (ESI) m/z 272.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08519134B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-f671b82318034f0cb789e824353d7fad |
|---|
| Source note | uspto-grants-2013_08 |
|---|