Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 22643158 | HCID 22643158 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22643263 | HCID 22643263 | — |
Reaction Steps
6-Nitro-4-chloro-2-(3-fluorophenyl)-quinoline 3.2 g (9.50 mmoles) was placed in a 250 mL three neck round bottom flask equipped with a condenser, magnetic stirrer, silicone oil heating bath, nitrogen inlet and gas outlet. To this was added 75 mL of N-methyl pyrrolidinone then 6.0 g (95 mmoles, 10 equiv.) of sodium azide. The mixture was stirred and warmed to 60° C. for 18 hr. After this time the mixture was cooled, poured into a 1 L separatory funnel containing 500 mL water and 250 mL of ethyl acetate. The pH was adjusted to 9.0 and the layers separated. The aqueous layer was extracted twice with 100 mL of ethyl acetate, the organic layers combined, dried over Na2SO4, filtered and concentrated to yield a product, which was carried to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06815447B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-9378255021c9464db75172fab67a1b9e |
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| Source note | uspto-grants-2004_11 |
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