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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640167Generated: October 31, 2026

Water → N-[4-chloro-3-(trifluoromethyl)phenyl]-7-{[2-(4,5-dihydro-1H-imidazol-2-yl)-pyridin-4-yl]oxy}-1,2,3,4-tetrahydronaphthalene-2-carboxamide

https://huagongshe.com/reaction/1640167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantN-[4-chloro-3-(trifluoromethyl)phenyl]-7-hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 58902317—
Reactant4-chloro-2-(4,5-dihydro-1H-imidazol-2-yl)pyridineHCID 59134959—
SolventDimethylformamideHCID 6228—
ProductN-[4-chloro-3-(trifluoromethyl)phenyl]-7-{[2-(4,5-dihydro-1H-imidazol-2-yl)-pyridin-4-yl]oxy}-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 2358521567.4%

Reaction Steps

To a solution of N-[4-chloro-3-(trifluoromethyl)phenyl]-7-hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxamide (64 mg, 0.17 mmol) and 4-chloro-2-(4,5-dihydro-1H-imidazol-2-yl)pyridine (35 mg, 0.19 mmol) in DMF (1.70 mL) was added Cs2CO3 (170 mg, 0.52 mmol). The mixture was irradiated in a microwave for 200 sec at 200° C. Water was added, and the mixture was extracted with EtOAc. The organic solution was washed with water (3×) and brine, dried over Na2SO4, filtered and evaporated. The residue was purified by column chromatography. The product was dissolved in MeOH, and 2.0M HCl in Et2O was added. The solvents were evaporated to give I-36 as a white solid (59 mg, 58%). 1H NMR (300 MHz, CD3OD): δ 8.62 (d, 1H), 8.17 (d, 1H), 7.82-7.78 (m, 1H), 7.63 (d, 1H), 7.53 (d, 1H), 7.25 (d, 1H), 7.21-7.18 (m, 1H), 6.96-6.91 (m, 2H), 4.11 (s, 4H), 3.14-2.82 (m, 5H), 2.24-2.16 (m, 1H), and 2.01-2.90 (m, 1H). LCMS: (FA) ES+ 516.2, ES− 513.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110687B2
Source datasetuspto-grants-2012_02
ORD IDord-9988032e1f5f40a898dd4443966accd6
Source noteuspto-grants-2012_02