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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373195Generated: November 2, 2026

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

https://huagongshe.com/reaction/1373195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllylamineHCID 7853—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoateHCID 58781115—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(allylamino)-3-fluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoateHCID 58781109—

Reaction Steps

A suspension of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-nitro-benzoic acid methyl ester (456.0 g, 1.008 mol) in a mixture of methanol (4.5 L), tetrahydrofuran (4.5 L) and water (1.13 L) was treated with allylamine (441.89 ml, 336.25 g, 5.88 mol) and stirred at room temperature for 30 min. (completion of reaction was confirmed by TLC-DCM:MeOH/9:1). The yellow colored suspension was filtered and washed with hexane to remove unreacted allylamine and dried to give the title compound as solid (yellow). Yield: 350g (50.90%), mp. 153–154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160915B2
Source datasetuspto-grants-2007_01
ORD IDord-7a7ce787382b446d9d622df419439d78
Source noteuspto-grants-2007_01