HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640903Generated: October 30, 2026
Hydrochloric Acid → HCID 178466653, compound
https://huagongshe.com/reaction/640903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-Acetyl-thiophene-2-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide | HCID 86610392 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178466653 | HCID 178466653 | 65% |
Reaction Steps
5-Acetyl-thiophene-2-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (1.245 g, 3.077 mmol) and ethyl formate (0.739 mL, 9.23 mmol) were dissolved in anhydrous ethanol (6.16 mL). The resulting solution was treated in dropwise fashion with a 21 wt % solution of sodium ethoxide in ethanol (5.75 mL, 15.38 mmol). This reaction mixture was heated at 78° C. for 1 h, producing a black oil. Subsequently, the reaction mixture was cooled to room temperature, and then the reaction pH was adjusted to pH 1 with dropwise addition of 1M HCl(aq) causing the formation of a pale orange precipitate. The suspension was filtered yielding an orange solid as the pure 5-Acetyl-thiophene-2-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.864 g, 1.99 mmol, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07692005B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-ed10ee843f9d4cc68083817b31a066c6 |
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| Source note | uspto-grants-2010_04 |
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