Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Picolinic acid | HCID 1018 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-chlorobenzoic acid | HCID 66646 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10402053 | HCID 10402053 | — |
Reaction Steps
Pyridine-2-carboxylic acid (369 mg, 3 mmol) was suspended in 15 ml dry toluene and diphenyl-phosphoryl azide (958 mg, 3.5 mmol) added. Triethylamine (354 mg, 3.6 mmol) was then added drop-wise and the mixture stirred at room temperature for 0.5 hour. The solution was heated to 80° C. and after 2 hours 2-amino-4-chloro-benzoic acid (463 mg, 2.7 mmol) was added in 20 ml THF and triethylamine (0.354 g, 3.6 mmol) was also added. The mixture was stirred for 1 hour at 80° C. and then at room temperature overnight. The mixture was allowed to cool and the solvent was removed under reduced pressure. The residue was taken up into ethyl acetate and precipitated with heptane and filtered with suction. Yield after recrystallation from ethyl acetate/heptane was 640 mg (73%) of white crystalline solid (m.p. 222-224° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521480B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-357f062ebe384ecebd50d608f4b7937f |
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| Source note | uspto-grants-2009_04 |
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