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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972215Generated: November 1, 2026

HCID 59485644, compound → HCID 59485721, compound

https://huagongshe.com/reaction/1972215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59485644HCID 59485644—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 59485721HCID 5948572183%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431607B2
Source datasetuspto-grants-2013_04
ORD IDord-ba80a0af185e45138648b357db1b812f
Source noteuspto-grants-2013_04