HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352964Generated: October 30, 2026
Hydrochloric Acid → HCID 178429651, compound
https://huagongshe.com/reaction/2352964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 86610464 | HCID 86610464 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178429651 | HCID 178429651 | 67.1% |
Reaction Steps
3-Methyl-thiophene-2-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.925 g, 2.4573 mmol) and ethyl formate (0.59 mL, 7.33 mmol) were dissolved in anhydrous ethanol (25 mL). The resulting solution was treated in dropwise fashion with a 21 wt % solution of sodium ethoxide in ethanol (4.583 mL, 12.28 mmol). This reaction mixture was heated at 78° C. for 0.5 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 tan precipitate. The suspension was filtered and the solids were washed with 0° C. EtOH to afford the pure 3-Methyl-thiophene-2-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.6659 g, 1.65 mmol, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749530B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-a5680c292a824711a7c74ae7c0bfcf3d |
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| Source note | uspto-grants-2010_07 |
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