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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036432Generated: October 30, 2026

Tetrahydrofuran → HCID 67413236, compound

https://huagongshe.com/reaction/1036432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDi-tert-butyl diethylphosphoramiditeHCID 4251849—
ReactantHCID 67414344HCID 67414344—
ReactantHCID 178418441HCID 178418441—
SolventDichloromethaneHCID 6344—
ProductHCID 67413236HCID 6741323682.4%

Reaction Steps

To a solution of {(R)-1-[6-(4-Cyclopentyl-cyclohexyloxy)-5-trifluoromethyl-naphthalen-2-yl]-2-hydroxy-1-methyl-ethyl}-carbamic acid tert-butyl ester (11 mg, 0.000020 mol) and 1H-tetrazole (14 mg, 0.00020 mol) in tetrahydrofuran (3 mL, 0.04 mol) was added di-tert-butyl N,N-Diethylphosphoramidite (28 μL, 0.00010 mol) at RT. The reaction was then quenched with 10% NaS2O3 in saturated sodium bicarbonate, extracted with EtOAc, washed with saturated sodium chloride and then dried with Na2SO4. The drying agent was filtered and the organic layer was concentrated under vacuum, yielding the crude product. The crude was taken up in DCM and purified using silica gel chromatography (24 g column), 0-100% ethyl acetate in hexanes) to give 12 mg of the desired compound as a white solid (77%). ESI-MS: 728 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ=8.18-8.08 (m, 1H), 7.92 (d, J=9.0 Hz, 1H), 7.63-7.42 (m, 2H), 7.22 (dd, J=5.0, 9.0 Hz, 1H), 4.32-4.11 (m, 1H), 3.98-3.80 (m, 2H), 2.18-1.98 (m, 2H), 1.92-0.71 (m, 46H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546359B2
Source datasetuspto-grants-2013_10
ORD IDord-ec36adc6874b449bbe0ee7ffc7184a9f
Source noteuspto-grants-2013_10