HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(5-Amino-6-chloro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(6-Chloro-5-nitro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate | HCID 59515906 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Amino-6-chloro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate | HCID 59515676 | — |
Reaction Steps
A round bottom flask was charged with 2-(6-chloro-5-nitro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate (450.00 mg, 0.0014484 mol), ethanol (20 mL, 0.3 mol) and ammonium chloride (774.8 mg, 0.01448 mol) in water (10 mL, 0.6 mol) was added at 85° C. followed by iron (324 mg, 0.00579 mol) in two portions. The reaction was stirred at that temperature for 45 minutes and then poured into methylene chloride (200 mL) and extracted. The solvent was removed to give the pure product as a light yellow solid. MS m/z=281.3 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816371B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-3b141c89002d4c47a1b2b8eee96c1bbe |
| Source note | uspto-grants-2010_10 |