HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370652Generated: October 30, 2026
Sodium Hydroxide → N4-(tert-butyloxycarbonyl)-N3-[4-(4-pyridyl)benzoyl]-3,4-pyridinediamine
https://huagongshe.com/reaction/1370652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Amino-4-(Boc-amino)pyridine | HCID 11095863 | — |
| Reactant | Sodium 4-(pyridin-4-yl)benzoate | HCID 23673507 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N4-(tert-butyloxycarbonyl)-N3-[4-(4-pyridyl)benzoyl]-3,4-pyridinediamine | HCID 12069544 | 10% |
Reaction Steps
A suspension of sodium 4-(4-pyridyl)benzoate (425 mg, 1.92 mmol) in methylene chloride was treated with oxalyl chloride (0.840 mL, 9.60 mmol), followed by dimethylformamide (0.01 mL)). After 0.75 h, the mixture was concentrated in vacuo. The residue was then dissolved in methylene chloride and added dropwise to a solution of N4-(tert-butyloxycarbonyl)-3,4-pyridinediamine (400 mg, 1.92 mmol) and pyridine (0.31 mL) in methylene chloride (2 mL) and tetrahydrofuran (1 mL). After 16 h, the mixture was poured into ethyl acetate and 1 N aqueous sodium hydroxide. The organic layer was washed once with 1 N aqueous sodium hydroxide, once with saturated sodium chloride solution, dried (potassium carbonate), and filtered. The residue was purified by flash chromatography (silica gel, ethyl acetate/hexanes) to yield 75 mg (10%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583173B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-3ee8b9d9b86540bda4e9152f046e212f |
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| Source note | uspto-grants-2003_06 |
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