Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| Reactant | 3-Aminophenylboronic acid monohydrate | HCID 14389423 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18957888 | HCID 18957888 | — |
Reaction Steps
. A mixture of 2-chloro-3-nitropyridine (5.0 g, 32.2 mmol), 3-aminophenylboronic acid monohydrate (5.11 g, 32.2 mmol), sodium carbonate (13.7 g, 32.2 mmol), and DMF (100 ml) was stirred at 100° C. for 1 h. After cooling to room temperature, ethyl acetate (500 ml) was added and the solids were filtered off. The solution was transferred to a separatory funnel and washed with aqueous hydrochloric acid (3×200 ml, 1M). The organic phase was dried and the solvent removed. Yield 6.5 g, mp 242°-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05360809 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-8c3606f24adf4debbc2facd27de717d6 |
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| Source note | uspto-grants-1994_11 |
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