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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729500Generated: October 31, 2026

2-Aminopyridine → HCID 57832788, compound

https://huagongshe.com/reaction/729500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
Reactant4931-36-6HCID 12909839—
SolventPyridineHCID 1049—
ProductHCID 57832788HCID 5783278874%

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582636B2
Source datasetuspto-grants-2009_09
ORD IDord-058ca0d1d56e4ff79cacecd226266326
Source noteuspto-grants-2009_09