HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(1-Methyl-3-isoquinolinyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15426261 | HCID 15426261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-Methyl-3-isoquinolinyl)acetamide | HCID 68313216 | — |
Reaction Steps
Acetic anhydride (1.4 mL, 15 mmol) was added to a suspension of Example 141A (0.79 g, 5.0 mmol) and triethylamine (0.76 ml, 5.5 mmol) in CH2Cl2 (20 mL) at ambient temperature. The mixture was stirred for 3.5 hours, then the volatiles were removed under reduced pressure. The residue was chased with toluene (3×25 mL) and then concentrated under reduced pressure to provide the title compound. MS (ESI) m/z 201 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802711B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-623146ec92544aa08d37a3e6ca281e3a |
| Source note | uspto-grants-2014_08 |