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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422552Generated: November 2, 2026

Diisopropylethylamine → (S)-1-(1-{[2-chloro-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoate

https://huagongshe.com/reaction/2422552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Trifluoromethyl)pent-1-YN-3-YL 4-nitrobenzoateHCID 59774870—
Reactant7-(Azidomethyl)-2-chloro-4-(4-fluorophenyl)quinolineHCID 86621980—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
Product(S)-1-(1-{[2-chloro-4-(4-fluorophenyl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoateHCID 86621981—

Reaction Steps

A mixture of 7-(azidomethyl)-2-chloro-4-(4-fluorophenyl)quinoline (500 mg, 1.60 mmol), 1-ethyl-1-(trifluoromethyl)prop-2-yn-1-yl 4-nitrobenzoate (529 mg, 1.76 mmol), copper iodide (456 mg, 2.4 mmol) and diisopropylethylamine (1.4 mL, 8.04 mmol) in THF (10 mL) was stirred at rt for 16 h. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification on silica gel (eluting with EtOAc/hexanes, 4:6) gave the title compound. MS (+ESI): 614 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-987babdab24a43b3aa17ae2d94b48223
Source noteuspto-grants-2011_06