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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364136Generated: October 30, 2026

4-Pyridinemethanamine → HCID 58882895, compound

https://huagongshe.com/reaction/2364136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinemethanamineHCID 77317—
ReactantHCID 58882900HCID 58882900—
SolventEthanolHCID 702—
ProductHCID 58882895HCID 58882895—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of ethyl 7-benzyl-4-hydroxy-1-[4-(methylsulfonyl)benzyl]-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate (40 mg, 0.080 mmol) and 4-(aminomethyl)pyridine (122 μL, 1.2 mmol) in EtOH (1 mL) was heated at 120° C. in a sealed tube in a microwave for 30 min. The reaction mixture was concentrated at reduced pressure, reconstituted in CH2Cl2 and washed with a mixture of 1N HCl and brine. Drying and evaporation of the organic phase gave the product as a pale green solid: 1H NMR (CDCl3) δ 10.81 (1H, br t, J=6 Hz), 8.69 (2H, d, J=7 Hz), 8.65 (1H, d, J=1 Hz), 7.83 (2H, d, J=8 Hz), 7.76 (2H, d, J=6 Hz), 7.31 (3H, m), 7.19 (2H, d, J=8 Hz), 7.11 (1H, s), 7.03 (2H, m), 5.43 (2H, br s), 4.86 (2H, d, J=6 Hz), 4.08 (2H, s), 3.03 (3H, s); HRMS calcd for C30H26N4O5S+H+: 555.1702. Found: 555.1699.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-a9545714a42f420783a583d4ae40cfac
Source noteuspto-grants-2014_04