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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062090Generated: November 1, 2026

Sodium Iodide → HCID 66701114, compound

https://huagongshe.com/reaction/2062090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
Reactant5-(Chloromethyl)-2-(trifluoromethyl)pyridineHCID 2773810—
ReactantHCID 59707047HCID 59707047—
SolventDimethylformamideHCID 6228—
ProductHCID 66701114HCID 6670111498.8%

Reaction Steps

0.3 mmol 1-[(1-hydroxy-naphthalene-2-carbonyl)-amino]-cyclobutanecarboxylic acid ethyl ester (94 mg), 0.6 mmol cesium carbonate (196 mg) (0.75 mmol in case of non-benzylic halides, +1 eq. in case of hydrochlorides) and 0.03 mmol sodium iodide (4 mg) are stirred for 10 min in 3 ml dry DMF. 0.33 mmol 5-Chloromethyl-2-trifluoromethyl-pyridine (65 mg) (0.45 mmol in case of non-benzylic halides) is added and the mixture is stirred for 2 h at RT and then for 5 h at 80° C. The cooled mixture is filtered, the filter washed with 5 ml ethyl acetate, the filtrate diluted with 20 ml ethyl acetate and washed twice with 20 ml 5% brine. The organic phase is dried and evaporated to yield 140 mg of 1-{[1-(6-Tri-fluoromethyl-pyridin-3-ylmethoxy)-naphthalene-2-carbonyl]-amino}-cyclobutane-carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283479B2
Source datasetuspto-grants-2012_10
ORD IDord-ab0ccfb67f6e4dfd90632480aa990984
Source noteuspto-grants-2012_10