HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914529Generated: October 31, 2026
Triethylamine → (1S,2S)-1-(4-Fluoro-benzenesulfonyl)-pyrrolidine-2-carboxylic acid [1-(4'-trifluoromethyl-biphenyl-3-yl)-ethyl]-amide
https://huagongshe.com/reaction/1914529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | (2S)-1-(4-fluorobenzenesulfonyl)pyrrolidine-2-carboxylic acid | HCID 686685 | — |
| Reactant | (5)-1-(4'-Trifluoromethyl-biphenyl-3-yl)ethylamine hydrochloride | HCID 66832512 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1S,2S)-1-(4-Fluoro-benzenesulfonyl)-pyrrolidine-2-carboxylic acid [1-(4'-trifluoromethyl-biphenyl-3-yl)-ethyl]-amide | HCID 49832576 | 54% |
Reaction Steps
A mixture of (5)-1-(4′-trifluoromethyl-biphenyl-3-yl)ethylamine hydrochloride (75 mg, 0.25 mmol), (S)-1-(4-fluoro-benzenesulfonyl)-pyrrolidine-2-carboxylic acid (68 mg, 0.25 mmol), N-(3-dimethylamniopropyl)-N′-ethylcarbodiimide hydrochloride (71 mg, 0.37 mmol), 1-hydroxybenzotriazole (50 mg, 0.37 mmol) and DMF (2 mL) was added Et3N (0.10 mL, 0.75 mmol). After 12 h, MeOH (0.5 mL) was added to the reaction mixture and resulting solution was purified by preparative reverse-phase HPLC to afford (70 mg, 54%) of a white solid. MS (ESI): mass calcd. for C26H24F4N2O3S, 520.1; m/z found, 521.1 [M+H]+. 1H NMR (500 MHz, CDCl3) δ 7.93-7.87 (m, 2H), 7.79 (d, J=8.0, 2H), 7.73-7.66 (m, 3H), 7.54 (d, J=7.6, 1H), 7.49 (t, J=7.6, 1H), 7.44 (d, J=7.6, 1H), 7.35 (d, J=8.0, 1H), 7.30-7.23 (m, J=8.7, 1H), 5.27-5.11 (m, 1H), 4.11 (dd, J=8.9, 3.1, 1H), 3.71-3.60 (m, 1H), 3.26-3.15 (m, 1H), 2.28-2.17 (m, 1H), 1.91-1.75 (m, 1H), 1.74-1.64 (m, 2H), 1.60 (d, J=7.0, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614201B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-b78cb65b2eca415993a5cb6df7426d46 |
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| Source note | uspto-grants-2013_12 |
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