Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 7-Methoxyisoquinoline | HCID 594375 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22631312 | HCID 22631312 | — |
Reaction Steps
5.6 g (35.2 mmol) of 7-methoxyisoquinoline was dissolved in 200 ml of xylene. 26.6 ml (176 mmol) of N,N,N′,N′-tetramethylenediamine and 7.28 g (186 mmol) of sodium amide were added to the obtained solution, and they were stirred at 140° C. for 1 hour. After the treatment with ethyl acetate as the extracting solvent in an ordinary manner, 50 ml of hydrobromic acid was added to the obtained crude product and they were stirred at 140° C. overnight. The solvent was evaporated to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825181B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-76c78ed82a0140428a57601dd43e3d4f |
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| Source note | uspto-grants-2004_11 |
|---|