HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzaldehyde → HCID 59774812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 59774845 | HCID 59774845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59774812 | HCID 59774812 | — |
Reaction Steps
To [5-phenoxy-1H-pyrrolo[2,3-b]pyridine (P-0035, 80 mg, 0.38 mol) in methanol (2.0 mL), 2,4-dichloro-benzaldehyde (32, 133 mg, 0.76 mmol) and potassium hydroxide (74 mg, 1.3 mmol) were added. The reaction was stirred at room temperature for 2 hours. The reaction mixture resulted in a precipitate, which was collected with vacuum filtration to provide the compound (33, 104 mg, 71%). MS (ESI) [M+H+]+=385.1 and 387.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268858B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-cd60ce9e18e2455f9e592f39dfd5f657 |
| Source note | uspto-grants-2012_09 |