HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093945Generated: November 1, 2026
Ethyl trifluoromethanesulphonate → HCID 59623724, compound
https://huagongshe.com/reaction/1093945
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trifluoromethanesulphonate | HCID 67924 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59623721 | HCID 59623721 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59623724 | HCID 59623724 | — |
Reaction Steps
To a solution of 3-(2-chloro-5-trifluoromethyl-phenylmethanesulfonylamino)-pyrazine-2-carboxylic acid methyl ester (Example 2.1) (1.5 g) in acetonitrile (20 ml) was added N,N-diisopropylethylamine (“Hunig's base”) (0.71 ml) at ambient temperature. The mixture was stirred for 5 minutes at ambient temperature before dropwise addition of a solution of ethyltrifluoromethanesulfonate (0.71 ml) in acetonitrile (5 ml) at ambient to temperature. The reaction mixture was stirred at ambient temperature for 4 hours. The reaction mixture was concentrated and the residue purified by column chromatography on silica gel (eluent: dichloromethane) to give 3-[(2-chloro-5-trifluoromethyl-phenyl-methanesulfonyl)-ethyl-amino]-pyrazine-2-carboxylic acid methyl ester as a beige solid (0.968 g). 1H-NMR (400 MHz, CDCl3): 8.57 (d, 1H), 8.52 (d, 1H), 7.77 (m, 1H), 7.50-7.56 (m, 2H), 4.64 (m, 2H), 4.01 (q, 2H), 4.00 (s, 3H), 1.23 (t, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133849B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-1d86ff2072be40fcafd87033f5f466a2 |
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| Source note | uspto-grants-2012_03 |
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