HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073211Generated: November 2, 2026
Iodoethane → Ethyl 2-methylbenzo[d]imidazo[2,1-b]thiazole-3-carboxylate
https://huagongshe.com/reaction/1073211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13118865 | HCID 13118865 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-methylbenzo[d]imidazo[2,1-b]thiazole-3-carboxylate | HCID 13118859 | 59.5% |
Reaction Steps
Subsequently, 6.0 g of 2-methylimidazo[2,1-b]benzothiazole-3-carboxylic acid was suspended in 100 ml of dry dimethylformamide. Under ice cooling, 1.5 g of 60% sodium hydride was added to the suspension. After stirring for 30 minutes, 6.0 g of ethyl iodide was added to the mixture followed by heating at 40° C. overnight. After completion of the reaction, the solvent was removed under reduced pressure. Ether and water were added to the residue, which was fractionated. The residue obtained from the ether phase was crystallized with n-hexane to give 4.0 g of ethyl 2-methylimidazo[2,1-b]benzothiazole-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968708 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-4f5eed6b59a64e7c8e4e621b3e391e2d |
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| Source note | uspto-grants-1990_11 |
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