HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668992Generated: October 30, 2026
3'-Aminoacetophenone → HCID 67338914, compound
https://huagongshe.com/reaction/1668992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3'-Aminoacetophenone | HCID 7417 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 86614221 | HCID 86614221 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 67338914 | HCID 67338914 | 24.2% |
Reaction Steps
To a solution of 1-chloro-5-iodo-6-methylphthalazine (0.380 g, 1.25 mmol) in IPA (3.0 ml), charged to a 5 mL microwave reaction vessel, 3′-aminoacetophenone (0.253 g, 1.87 mmol) was added. The reaction mixture was stirred at 160° C. for 15 min. The reaction mixture was diluted with excess DCM and saturated aqueous sodium bicarbonate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated under vacuum. The resulting residue was loaded on to silica and purified by column chromatography. (ISCO 40.0 g, 10-70% EtOAc in Hex., 25 min.) to give 1-(3-(5-iodo-6-methylphthalazin-1-ylamino)phenyl)ethanone (0.122 g, 24.2% yield). MS (M+H)+ 404.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07989461B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-d2c66caa434e4aa79a35140be1c2eaf0 |
|---|
| Source note | uspto-grants-2011_08 |
|---|