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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842660Generated: October 31, 2026

Nicotinic acid, hydrazide → Quinoxaline

https://huagongshe.com/reaction/842660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic acid, hydrazideHCID 11112—
ReactantHCID 18726777HCID 18726777—
CatalystMercuric oxideHCID 30856—
Solvent1,4-DioxaneHCID 31275—
ProductQuinoxalineHCID 7045127.5%

Reaction Steps

A mixture of 6,7-dichloro-2,3-dimethoxy-5-methoxythioacetamidoquinoxaline (25.3 g, 69.9 mmol), nicotinic acid hydrazide (19.3 g, 140.8 mmol), mercury(II) oxide (15.1 g, 69.7 mmol) and 1,4-dioxane (600 mL) was heated under reflux for 18 hours. After cooling, the mixture was filtered through ARBOCEL (trade mark) filter aid and the residue washed with dichloromethane. The filtrate was concentrated under reduced pressure to afford a light brown solid which was partitioned between ethyl acetate and 2M aqueous hydrochloric acid solution. The layers were separated and the aqueous layer was extracted with dichloromethane (2×500 mL, 4×100 mL). The combined dichloromethane extracts were dried (MgSO4) and concentrated under reduced pressure. The residue was crystallised from ethyl acetate/methanol to give (±)-6,7-dichloro-2,3-dimethoxy-5-[3-methoxymethyl-5-(3-pyridyl)-4H-1,2,4-triazol-4-yl)]quinoxaline (11.6 g, 37%) as a pale yellow solid, mp 189-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376490B1
Source datasetuspto-grants-2002_04
ORD IDord-08995db5a3e242ce844b5833df02f266
Source noteuspto-grants-2002_04