HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045635Generated: November 1, 2026
Potassium Carbonate → 3-(2-Chloro-5-trifluoromethyl-benzylsulfanylmethyl)-pyrazine-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1045635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Bromomethyl)-1-chloro-4-(trifluoromethyl)benzene | HCID 2736685 | — |
| Reactant | 3-Carbamimidoylsulfanylmethyl-pyrazine-2-carboxylic acid ethyl ester hydrobromide | HCID 66788977 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Chloro-5-trifluoromethyl-benzylsulfanylmethyl)-pyrazine-2-carboxylic acid ethyl ester | HCID 66788811 | — |
Reaction Steps
To a solution of 3-carbamimidoylsulfanylmethyl-pyrazine-2-carboxylic acid ethyl ester hydrobromide (0.367 g) in acetonitrile (2 ml) was added 2-chloro-5-trifluoromethyl-benzylbromide (commercially available) (0.294 g), potassium carbonate (0.316 g) and water (3 drops). The reaction mixture was heated to 120° C. for 10 minutes in the microwave. The reaction mixture was filtered and the filtrate concentrated. The residue was purified by chromatography on silica gel (eluent: 0-10% v/v ethyl acetate in iso-hexane) to give Compound No. A2 of Table A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569301B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-94eaf54777c0444d8e4724121390778d |
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| Source note | uspto-grants-2013_10 |
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