HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamidine monohydrochloride → HCID 178433414, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-Methyl-2-oxo-3-phenyl-cyclohexanecarboxylic acid methyl ester | HCID 58866053 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433414 | HCID 178433414 | 52.4% |
Reaction Steps
A solution of potassium t-butoxide (8.4 g, 75 mmol), acetamidine hydrochloride (7.1 g, 75 mmol) and 3-methyl-2-oxo-3-phenyl-cyclohexanecarboxylic acid methyl ester (30 mmol) in 150 mL of ethanol was stirred at room temperature for 12 hours and then heated under reflux for 2 hours. The mixture was concentrated under reduced pressure, diluted with water, and washed with ether. The aqueous layer was neutralized with HCl and filtered to afford 4.0 g of 2,8-dimethyl-8-phenyl-5,6,7,8-tetrahydro-quinazolin-4-ol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223767B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-3320c159821641c49fc499b71acd4f24 |
| Source note | uspto-grants-2007_05 |