HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098295Generated: November 1, 2026
Chloroacetyl chloride → HCID 23156812, compound
https://huagongshe.com/reaction/1098295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23156743 | HCID 23156743 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 23156812 | HCID 23156812 | 86.1% |
Reaction Steps
0.236 ml (1.69 mmol) of triethylamine and 0.101 ml (1.27 mmol) of chloroacetyl chloride were added in this order to 200 mg (0.85 mmol) of 7-amino-3-phenyl-2H-isoquinolin-1-one obtained in Example 39. The obtained mixture was stirred at a room temperature for 2 hours. Thereafter, 30 ml of 1 N hydrochloric acid was added to the reaction solution, and the mixture was then extracted with methylene chloride (30 ml×2). The extract was dried over anhydrous magnesium sulfate, and the solvent was then distilled away under reduced pressure. The precipitated solid was collected by filtration, and the filtrate was then washed with a suitable amount of ether, so as to obtain 229 mg (86%) of 2-chloro-N-(1-oxo-3-phenyl-1,2-dihydroisoquinolin-7-yl)acetamide in the form of a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08143274B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-37990939d81a4613838e7fa5843b3d4f |
|---|
| Source note | uspto-grants-2012_03 |
|---|