HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926613Generated: October 29, 2026
Ammonium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide
https://huagongshe.com/reaction/1926613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid | HCID 58022862 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide | HCID 58022896 | — |
Reaction Steps
To a suspension of 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.85 g, 7.93 mmol) in methylene chloride (30 mL), were added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (3.28 g, 17.1 mmol) and 1-hydroxybenzotriazole (2.27 g, 16.8 mmol). The reaction mixture was stirred at room temperature for two hours and ammonium hydroxide (15.4 mL) was added and the biphasic mixture was stirred at room temperature for two hours. Water (100 mL), methanol (50 mL), methylene chloride (200 mL) was added. The organic layer was removed. The aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to the title compound as dark red oil (1.47 g, 57%). LCMS: (FA) ES+ 325.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08183240B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-a14852fab0c84029b92e00c336c5927f |
|---|
| Source note | uspto-grants-2012_05 |
|---|