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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161784Generated: October 29, 2026

Methanol → Methyl 4-(allylamino)-3-fluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoate

https://huagongshe.com/reaction/1161784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantAllylamineHCID 7853—
ReactantMethyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoateHCID 58781115—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(allylamino)-3-fluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoateHCID 58781109—

Reaction Steps

A suspension of methyl 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoate (3.9 g, 8.62 mmoles) and allylamine (3.5 ml, 43 mmoles) in a mixture of THF (10 ml), MeOH (10 ml) and H2O (2.5 ml) is stirred at room temperature for 30 min. The yellow suspension is filtered and washed with hexane to remove the excess of allylamine. The resulting solid is dried under vacuum to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820664B2
Source datasetuspto-grants-2010_10
ORD IDord-af9d7ea2af7b42e38cd680fccb76e87a
Source noteuspto-grants-2010_10