HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178464127, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178422250 | HCID 178422250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178464127 | HCID 178464127 | — |
Reaction Steps
A reaction mixture consisting of 150 mg (0.49 mmol) 6-(cis-4-amino-cyclohexyloxy)-7-methyl-2H-isoquinolin-1-one hydrochloride (example 138), 38 mg (0.63 mmol) of acetic acid, 43 mg (0.97 mmol) of acetaldehyde, molecular sieves and 515 mg (2.4 mmol) of sodium triacetoxy borohydride in 5 ml of methylene chloride was stirred overnight. The reaction mixture was added to 10 ml of 1 M sodium hydroxide solution and extracted twice with a mixture of methylene chloride and isopropanol. After drying and evaporation 122 mg of 6-(cis-4-diethylamino-cyclohexyloxy)-7-methyl-2H-isoquinolin-1-one (146) were obtained. Rt=0.99 min (Method B). Detected mass: 329.17 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609691B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-71d4999898734e1cb6e57e3f2715c2bb |
| Source note | uspto-grants-2013_12 |