HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972215Generated: November 1, 2026
HCID 59485644, compound → HCID 59485721, compound
https://huagongshe.com/reaction/1972215
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59485644 | HCID 59485644 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 59485721 | HCID 59485721 | 83% |
Reaction Steps
A solution of (S)-2-(3-(4-(4-chlorophenoxy)phenyl)-2-oxo-4-(3-(trifluoromethyl)-phenyl)imidazolidin-1-yl)-N,N-bis(4-methoxybenzyl)ethanesulfonamide (2.2 g, 2.82 mmol) in TFA (30 mL) is stirred at room temperature for 14 h. Excess of TFA is removed under vacuum. The residue is treated with saturated NaHCO3 aqueous solution (30 mL) and extracted with EtOAc (3×50 mL). The combined organic layer is washed with brine and dried (MgSO4). After removing the drying agent, the solution is concentrated and purified by flash column chromatography (silica gel, EtOAc/hexane 0%˜90%) to provide the desired product (S)-2-(3-(4-(4-chlorophenoxy)phenyl)-2-oxo-4-(3-(trifluoromethyl)phenyl)-imidazolidin-1-yl)ethanesulfonamide as white solid (1.2 g, 83%). 1H NMR (CDCl3, 400 MHz) δ 7.55˜7.62 (m, 3H), 7.48 (t, 1H), 7.24 (d, 2H), 7.22 (d, 2H), 6.85 (m, 4H), 5.47 (s, 2H), 5.28 (dd, 1H), 3.90˜4.03 (m, 3H), 3.40 (dd, 1H), 3.28˜3.35 (m, 2H); HPLC-MS calculated for C24H21ClF3N3O4S (M+H+) 540.1, found 540.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431607B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-ba80a0af185e45138648b357db1b812f |
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| Source note | uspto-grants-2013_04 |
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