HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476817Generated: October 30, 2026
Acetic Acid → Ethyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate
https://huagongshe.com/reaction/1476817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Reactant | Methyl 5-chloro-2-formylbenzoate | HCID 58437623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate | HCID 90386855 | 31.8% |
Reaction Steps
To a stirred mixture of NaH (1.81 g, 30.3 mmol) in DMF (20 mL) was added a solution of methyl 5-chloro-2-formylbenzoate (5.0 g, 25 mmol) and ethyl 2-isocyanoacetate (2.85 g, 25 mmol) in DMF (60 mL) at 40° C. over a 20 minute period. The reaction mixture was stirred at 20° C. for 2 hours. Its pH was adjusted to 7.0 with acetic acid (10%) and the mixture was extracted with DCM (3×200 mL). The organic layers were combined, washed with brine (200 mL), dried over Na2SO4, and concentrated. The crude product was purified by silica gel column chromatography eluting with petroleum ether and ethyl acetate (PE/EtOAc=15:1-5:1 gradient) to give the title compound (2.0 g, 31%). ESI-MS m/z [M+H]+252.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09402841B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-02530edde588415687a8ebb6df7b5fc2 |
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| Source note | uspto-grants-2016_08 |
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