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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523520Generated: October 25, 2026

Hydrochloric Acid → 4-Iodo-3-(2-methyl-acryloylamino)-benzoic acid methyl ester

https://huagongshe.com/reaction/523520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethacrylic AcidHCID 4093—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantMethyl 3-amino-4-iodobenzoateHCID 21628210—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-Iodo-3-(2-methyl-acryloylamino)-benzoic acid methyl esterHCID 68482337—

Reaction Steps

To a stirred suspension of Methyl 3-amino-4-iodobenzoate (1.67 g, 6 mmol) and Methacrylic acid (568 mg, 6.6 mmol) in dichloromethane (60 mL) and DMF (60 mL) were added O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) (2.5 g, 6.6 mmol) and then a solution of N,N-diisopropylethylamine (1.16 g, 1560 pt, 9 mmol) in DMF (20 mL). The reaction mixture was stirred at ambient temperature for 24 h. The reaction medium was acidified by adding a 1.2 M hydrochloric acid solution and extracted with ethyl acetate. The organic phase was washed with water, dried (MgSO4), and concentrated to give the amide which was purified by flash chromatography (AcOEt/heptane: 5/5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339486B2
Source datasetuspto-grants-2016_05
ORD IDord-3c65323397064e7ba7f03129f1b038b2
Source noteuspto-grants-2016_05