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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351176Generated: November 1, 2026

Formic Acid → HCID 11749456, compound

https://huagongshe.com/reaction/1351176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21098407HCID 21098407—
SolventChloroformHCID 6212—
ProductHCID 11749456HCID 11749456—

Reaction Steps

A solution of N4-(3-bromo-phenyl)-6,7-dimethoxy-quinazoline-4,5-diamine (100 mg, 0.27 mmol) (from Example 6, Step B supra) in formic acid (5 mL) was heated at 110° C. for 2 hours. Aqueous NaOH solution was added to the reaction mixture to a pH 10–12. The solution was diluted with chloroform (100 mL). The organic layer was separated, dried over Na2SO4, and concentrated. This residue was purified by chromatography using EtOAc/Et3N (1:0.04) as eluent to give the desired 3-(3-bromo-phenyl)-8,9-dimethoxy-3H-1,3,4,6-tetraaza-phenalene as a brown solid. (Yield 86 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-064f49130f0a46f298ea56d47849e766
Source noteuspto-grants-2007_05