HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485343Generated: October 29, 2026
Ethyl Thioglycolate → 3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indole
https://huagongshe.com/reaction/485343
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(3-pyridyl)indole 3-propyl benzenesulfonate | HCID 86740258 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indole | HCID 20270198 | — |
Reaction Steps
A solution of 0.36 g of ethyl mercaptoacetate in 20 ml of dimethylformamide is treated with 0.145 g of a 50% oil dispersion of sodium hydride at room temperature under nitrogen for 15 minutes. A solution of 1.13 g of N-(3-pyridyl)indole-3-propyl benzenesulfonate in 5 ml of dimethylformamide is added at room temperature. The reaction mixture is stirred for 15 hours, diluted with 100 ml of water and extracted 4 times with 50 ml of ethyl ether. The organic extracts are washed with 50 ml of water and 20 ml of cold 1N hydrochloric acid. The acid phase is extracted with ether and brought to pH=8.5 with 50% sodium hydroxide solution. The aqueous phase is extracted with chloroform (3×30 ml). The chloroform extract is dried over potassium carbonate and evaporated to yield 3-[3-(ethoxycarbonylmethylthio)propyl]-N-(3-pyridyl)indole; IR (CH2Cl2) 1725 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536505 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-521735bd8390406ea7297250b6ab968e |
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| Source note | uspto-grants-1985_08 |
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