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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76038Generated: October 29, 2026

HCID 66615893, compound → 4-(4-{4-[2-(3-Chlorophenylamino)-oxazol-5-yl]-phenyl}-cyclohexyl)-butyric acid

https://huagongshe.com/reaction/76038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66615893HCID 66615893—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanol ethylacetateHCID 21584252—
Product4-(4-{4-[2-(3-Chlorophenylamino)-oxazol-5-yl]-phenyl}-cyclohexyl)-butyric acidHCID 5789908886.1%

Reaction Steps

To a solution of (E)-4-(4-{4-[2-(3-chlorophenylamino)-oxazol-5-yl]-phenyl}-cyclohexyl)-but-2-enoic acid benzyl ester (139 mg, 0.283 mmol) in EtOAc/EtOH (5:1 v/v, 6 mL) is added Pd(OH)2 (100 mg) the mixture is stirred in an hydrogenated at 1 atm for 72 h. The catalyst is filtered and washed with EtOAc. The filtrated is then concentrated and dried under high vacuum to give the title compound (107 mg) as a white solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 0.98-1.09 (m, 2H) 1.18-1.25 (m, 2H) 1.39-1.48 (m, 2H) 1.49-1.57 (m, 2H) 1.82 (d, J=10.11 Hz, 4H) 1.74-1.85 (m, 1H) 2.18 (t, J=7-33 Hz, 2H) 6.99 (ddd, J=7.96, 2.02, 0.88 Hz, 1H) 7.28-7.33 (m, 3H) 7.40 (s, 1H) 7.47-7.52 (m, 3H) 7.85 (t, J=2.02 Hz, 1H); (M+H)+=439.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835451B2
Source datasetuspto-grants-2014_09
ORD IDord-89f72d33df90437bb9d09ebe8d4abe12
Source noteuspto-grants-2014_09