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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393358Generated: November 1, 2026

Ethanol → HCID 18974894, compound

https://huagongshe.com/reaction/2393358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-MethoxyanilineHCID 7000—
ReactantHCID 18974948HCID 18974948—
ProductHCID 18974894HCID 18974894—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Bromoacetyl-6-(4-chlorophenyl)-1-methyl-4H-2,3,4,5,10b-pentaazabenz[e]azulene (8 mg) obtained in Example 171 was suspended in ethanol and 2-anisidine (12.5 μl) was added. The mixture was stirred at 80° C. for 3 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. Water (20 ml) was added to the residue and the mixture was extracted with ethyl acetate (20 ml). The organic layer was further washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by preparative thin-layer chromatography to give 2.4 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807850
Source datasetuspto-grants-1998_09
ORD IDord-cb36be60f976412484c9c19b2d29e63c
Source noteuspto-grants-1998_09