HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272902Generated: October 30, 2026
Dimethylformamide → HCID 117974266, compound
https://huagongshe.com/reaction/2272902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium ethanethiol | HCID 45051917 | — |
| Reactant | HCID 117974059 | HCID 117974059 | — |
| Reactant | HCID 117974601 | HCID 117974601 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 117974266 | HCID 117974266 | 188% |
Reaction Steps
A mixture of 0.22 g of 2-(3-chlorothiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine, 0.23 g of 2-(3-bromothiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine, 0.21 g of ethyl mercaptan sodium salt (80%) and 4 ml of DMF was stirred at 100° C. for 30 minutes. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.41 g of 2-(3-ethylthiothiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention (15)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120792B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-879b455beebb41b2a52f52c758f3c692 |
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| Source note | uspto-grants-2015_09 |
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