HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250571Generated: October 25, 2026
1-(p-Methoxyphenyl)-2-propanone → 4-[7-Ethyl-3-(4-methoxyphenyl)-2-methylpyrrolo[1,2-b]pyridazin-4-yl]benzonitrile
https://huagongshe.com/reaction/2250571
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(p-Methoxyphenyl)-2-propanone | HCID 31231 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-[(1-amino-5-ethyl-1H-pyrrol-2-yl)carbonyl]benzonitrile | HCID 57444479 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[7-Ethyl-3-(4-methoxyphenyl)-2-methylpyrrolo[1,2-b]pyridazin-4-yl]benzonitrile | HCID 68802756 | 20.2% |
Reaction Steps
To a solution of 4-[(1-amino-5-ethyl-1H-pyrrol-2-yl)carbonyl]benzonitrile (100 mg) in toluene (1 mL) were added 1-(4-methoxyphenyl)acetone (103 mg) and p-toluene-sulfonic acid monohydrate (16 mg) at ambient temperature. The reaction mixture was heated at 80° C. for 3 hours. The mixture was evaporated in vacuo. The residue was purified by flash silica gel column chromatography eluting with hexane-ethyl acetate 20-1 and 15-1 to give 4-[7-ethyl-3-(4-methoxyphenyl)-2-methylpyrrolo[1,2-b]pyridazin-4-yl]benzonitrile (31 mg, 20.2%) as an yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07317009B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-6af94acd8f6143359173bf198fa8d7d6 |
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| Source note | uspto-grants-2008_01 |
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