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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289611Generated: October 31, 2026

2-Aminopyridine → HCID 15888360, compound

https://huagongshe.com/reaction/2289611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 10198942HCID 10198942—
SolventDichloromethaneHCID 6344—
ProductHCID 15888360HCID 1588836083.1%

Reaction Steps

To a cooled solution of 3-bromo-1,2,4-thiadiazolo[4,5-a]benzimidazole (0.30 g, 1.17 mmol) in 15 mL of dichloromethane, 2-aminopyridine (0.276 g, 2.93 mmol) was added dropwise and the mixture was allowed to stir for 48 h. The reaction mixture wad diluted with 100 mL of dichloromethane and washed with water (2×30 mL) and then brine (1×25 mL). The organic layer was dried over magnesium sulfate and evaporated to give a yellow solid (0.26 g, 83%) 1H-NMR (CDCl3) δ 6.59 (apparent 5, 1H, pyr-H), 7.12 (apparent br. d, 1H, pyr-H), 7.28 (t, 1H, ArH), 7.38 (t, 1H, ArH), 7.51 (m, 2H, ArH & pyr-H), 7.70 (d, 1H, ArH), 8.28 (d, 1H, pyr-H); m.p. 155.5-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093738
Source datasetuspto-grants-2000_07
ORD IDord-9b9c51d1c4ad4008871aa82b8b009009
Source noteuspto-grants-2000_07