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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-Iodomethylaniline | HCID 68678424 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-Iodo-4-methylphenyl)thiophene-3-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642276B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-8e6667ea2ec8496f899d3ac51963f8b0 |
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| Source note | uspto-grants-2010_01 |
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