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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257785Generated: November 1, 2026

2-Aminopyridine → HCID 5273632, compound

https://huagongshe.com/reaction/2257785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 19704106HCID 19704106—
SolventDimethylformamideHCID 6228—
ProductHCID 5273632HCID 527363244%

Reaction Steps

A solution of 1-(2-[2-methoxyphenyl]ethyl)thiocarbamoyl imidazole (0.52 g, 2 mmol ) and 2-aminopyridine (0.19 g, 2 mmol) in N,N-dimethylformamide (5 mL) was stirred at 90° C. for 4 h, the reaction was cooled to room temperature and the solvent removed in vacuo. The residue was crystallized from ethyl acetate to provide 0.25 g (44%) of the titled product: IR (KBr, cm-1) 3219, 3048, 1607, 1557, 1236, 1036, 756; 1H NMR (300 MHz, DMSO-d6) δ 11.65 (m, 1H), 10.55 (br s, 1H), 8.1 (m, 1H), 7.75 (m, 1H), 7.3-6.9 (m, 6H), 3.8 (m, 2H), 3.78 (s, 3H), 2.9 (t, J=7 Hz, 2H); MS (FD) m/e 287 (M+) ; UV (EtOH) 290 nm (ε=10141), 267 nm (ε=13121), 247 nm (ε=10959), 202 nm (ε=24078).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658907
Source datasetuspto-grants-1997_08
ORD IDord-68d631888e7e4042982527ef7e0c0458
Source noteuspto-grants-1997_08