HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729500Generated: October 31, 2026
2-Aminopyridine → HCID 57832788, compound
https://huagongshe.com/reaction/729500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| Reactant | 4931-36-6 | HCID 12909839 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57832788 | HCID 57832788 | 74% |
Reaction Steps
2-Aminopyridine was converted to 1,2-diaminopyridinium iodide from a known literature method (J. Org. Chem., 31:260-265 (1996)). 1,2-Diaminopyridinium iodide (0.270 g, 1.1 mmol) was treated with 4-tert-butyl-benzoyl chloride (0.432 g, 2.2 mmol) in pyridine (2 mL). The reaction was heated at 85° C. in a sealed tube for 3 h, at which time the mixture was cooled to room temperature. The reaction was partitioned between ethyl acetate (50 mL) and water (50 mL). The ethyl acetate extract was dried over magnesium sulfate and concentrated. The crude material was purified by flash silica gel chromatography, eluting with 25% ethyl acetate/hexanes (Rf=0.4) to yield 0.205 g (74%) of the purified product. MS (ES) m/z 252.2; HPLC (Method B): r.t.=6.7 min., purity 100% at 210-370 nm, 100% at 254 nm. HRMS: calcd for C16H17N3+H+, 252.14952; found (ESI, [M+H]30 ), 252.149.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582636B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-058ca0d1d56e4ff79cacecd226266326 |
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| Source note | uspto-grants-2009_09 |
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