HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823931Generated: October 30, 2026
1-Phenyl-1,2-propanedione → 3-(5-methyl-4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline
https://huagongshe.com/reaction/1823931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenyl-1,2-propanedione | HCID 11363 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate | HCID 12190329 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(5-methyl-4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline | HCID 21914142 | — |
Reaction Steps
3-Formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (1.83 g, 7 mmol) was combined with AcOH (25 mL) to which was immediately added 1-phenyl-propane-1,2-dione (3.11 g, 21 mmol) and NH4OAc (13.49 g, 175 mmol). The reaction mixture was then placed on a steam bath and heated under an argon atmosphere for 20 minutes. The reaction mixture was cooled in an ice bath and then added to an ice slurry (44 g). The resulting mixture was basified by addition of concentrated NH4OH (50 mL) and then extracted twice with diethyl ether (150 mL each). The combined organic phases were dried over MgSO4, filtered and concentrated to yield crude product. This material was purified by preparative HPLC to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07041681B2 |
|---|
| Source dataset | uspto-grants-2006_05 |
|---|
| ORD ID | ord-7647c46102f94ab582024f138e0c065e |
|---|
| Source note | uspto-grants-2006_05 |
|---|