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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735895Generated: October 26, 2026

Cyclopentyl 4-trifluoromethylphenyl ketone → N-{cyclopentyl[4-(trifluoromethyl)phenyl]methyl}-N-[4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzyl]amine

https://huagongshe.com/reaction/735895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentyl 4-trifluoromethylphenyl ketoneHCID 24724174—
ReactantHCID 67187547HCID 67187547—
ProductN-{cyclopentyl[4-(trifluoromethyl)phenyl]methyl}-N-[4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzyl]amineHCID 6718725555%

Reaction Steps

The same procedure as employed in the preparation of Example 223 (step b) but using cyclopentyl[4-(trifluoromethyl)phenyl]methanone and 4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzylamine gave the title compound as a colorless oil (55%). 1H NMR (DMSO-d6, 300 MHz) δ 8.00 (d, 2H), 7.64 (m, 2H), 7.50 (m, 4H), 3.62-3.34 (m, 2H), 2.74 (m, 2H), 2.12-1.85 (m, 2H), 1.70 (m, 2H), 1.60-0.92 (m, 25H), 0.83 (m, 3H). HPLC (Condition A), Rt: 5.42 min (HPLC purity: 98.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592477B2
Source datasetuspto-grants-2009_09
ORD IDord-91986d5eeee14f3b89cc3196d709d02a
Source noteuspto-grants-2009_09