HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418489Generated: October 26, 2026
Ethanol → (R)-2-(5-Amino-6-chloro-1-oxoisoquinolin-2(1H)-yl)propanamide
https://huagongshe.com/reaction/418489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (R)-2-(6-Chloro-5-nitro-1-oxoisoquinolin-2(1H)-yl)propanamide | HCID 59515858 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-2-(5-Amino-6-chloro-1-oxoisoquinolin-2(1H)-yl)propanamide | HCID 59515791 | — |
Reaction Steps
To a solution of (R)-2-(6-chloro-5-nitro-1-oxoisoquinolin-2(1H)-yl)propanamide (120 mg, 0.00040 mol) in ethanol (4 mL, 0.07 mol) was added ammonium chloride (200 mg, 0.004 mol) in water (4 mL, 0.2 mol). The reaction was heated at 85° C. and iron (90 mg, 0.002 mol) was added in two portions 5 minutes apart. The reaction was stirred for 30 minutes and ethyl acetate was added and decanted. the solvent was removed under reduced pressureunder reduced pressure to afford the product as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093265B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-7e76d2f10efd49289595eccef508528c |
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| Source note | uspto-grants-2012_01 |
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