Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azepane | HCID 8119 | — |
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 16775581 | HCID 16775581 | — |
Reaction Steps
A suspension of 6-chloronicotinic acid (5.0 g) and perhydroazepine (7.16 mL) in xylene (20 mL) was stirred at 140° C. for 30 hours under an atmosphere of argon. The reaction mixture was cooled to room temperature, diluted with hexane and filtrated. The insoluble material was dissolved in ethyl acetate. The organic layer was washed with water and brine sequentially, dried over anhydrous magnesium sulfate and concentrated to give the title compound (3.19 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323456B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-ad77aa8a2aec48039e6839591256fd0f |
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| Source note | uspto-grants-2008_01 |
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