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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988876Generated: October 26, 2026

Thiophene-3-carboxylic acid → N-(3-Iodo-4-methylphenyl)thiophene-3-carboxamide

https://huagongshe.com/reaction/1988876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-3-carboxylic acidHCID 6918—
Reactant1-HydroxybenzotriazoleHCID 75771—
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—
Reactant3-IodomethylanilineHCID 68678424—
SolventDimethylformamideHCID 6228—
ProductN-(3-Iodo-4-methylphenyl)thiophene-3-carboxamideHCID 21914512—

Reaction Steps

Thiophene-3-carboxylic acid (2.75 g) and HATU (8.15 g) in DMF (25 ml) were stirred at room temp for 15 min. HOBT (2.9 g), 3-iodomethylaniline (5.0 g) and DIPEA (11.2 ml, 64.35 mmol) were added and the reaction was stirred at room temp for 16 h. The solvent was evaporated under vacuum and the residue was partitioned between ethyl acetate (100 ml) and aqueous sodium carbonate (10%, 100 ml). The aqueous layer was extracted with ethyl acetate (50 ml) and the combined organic phases washed with hydrochloric acid (2N, 75 ml), water (75 ml) and brine (75 ml). The organic phase was dried (magnesium sulphate) and absorbed onto silica. The silica was applied to a silica column and eluted with cyclohexane/ethyl acetate (4:1). The solvent was evaporated from the product fractions under vacuum to the tide compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642276B2
Source datasetuspto-grants-2010_01
ORD IDord-8e6667ea2ec8496f899d3ac51963f8b0
Source noteuspto-grants-2010_01