HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161251Generated: October 30, 2026
Water → Methyl 2-(5-amino-1-oxoisoquinolin-2(1H)-yl)-2-(4-chlorophenyl)acetate
https://huagongshe.com/reaction/1161251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2-(4-chlorophenyl)-2-(5-nitro-1-oxoisoquinolin-2(1H)-yl)acetate | HCID 58973969 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(5-amino-1-oxoisoquinolin-2(1H)-yl)-2-(4-chlorophenyl)acetate | HCID 58973946 | — |
Reaction Steps
A round bottom flask was charged with methyl 2-(4-chlorophenyl)-2-(5-nitro-1-oxoisoquinolin-2(1H)-yl)acetate (4.2 g, 0.011 mol) ethanol (60 mL, 1 mol) and ammonium chloride (6 g, 0.1 mol) in water (60 mL, 3 mol) was added and the reaction heated at 80° C. and iron (2 g, 0.04 mol) was added in four portions 5 minutes apart. The reaction was heated for another 1 h at that temperature and cooled to room temperature and poured into 200 ml dichloromethane and extracted. The solvent was removed to obtain the product as a light brown solid. MS m/z=343.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816371B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-eea26390a0484865a5608c8b63455ad8 |
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| Source note | uspto-grants-2010_10 |
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