HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234085Generated: October 30, 2026
Acetyl chloride → 4-(3-acetyl-1H-indol-2-yl)-6-pyridin-4-yl-2H-pyridazin-3-one
https://huagongshe.com/reaction/2234085
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-1H-indole trifluoroacetate | HCID 23092453 | — |
| Reactant | Aluminium chloride 1,2-dichloroethane | HCID 86612051 | — |
| Product | 4-(3-acetyl-1H-indol-2-yl)-6-pyridin-4-yl-2H-pyridazin-3-one | HCID 135489493 | 48.1% |
Reaction Steps
4 mg acetyl chlorid are added at 0° C. to a suspension of 80 mg aluminium chloride 1,2-dichloroethane, followed by 208 mg 2-(3-Methoxy-6-pyridin-4-yl-pyridazin-4-yl)-1H-indole trifluoroacetate. The reaction mixture is stirred for 4 h at room temperature and for 3 h at 50° C. It is worked up pouring into an ice/water mixture and filtration. The layers are separated, the organic is layer washed with Water, dried over MgSO4 and the solvent removed. Reversed phase HPLC chromatography yielded 8.1 mg 4-(3-acetyl-1H-indol-2-yl)-6-pyridin-4-yl-2H-pyridazin-3-one
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07709466B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-3512d65c19f448c4bab2e1505feaca8b |
|---|
| Source note | uspto-grants-2010_05 |
|---|