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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714267Generated: October 29, 2026

Diisopropylcarbodiimide → HCID 56948654, compound

https://huagongshe.com/reaction/714267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 43165089HCID 43165089—
ReactantHCID 66824535HCID 66824535—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 56948654HCID 5694865416.64%

Reaction Steps

To a solution of 3-(1-(3,5-difluorophenyl)cyclohexyl)propanoic acid (20 mg, 0.075 mmol) and (Z)—N′-hydroxy-2-oxo-1,2-dihydropyridine-4-carboximidamide (11.42 mg, 0.075 mmol) in acetonitrile (1 mL) was added N,N′-diisopropylcarbodiimide (0.013 mL, 0.082 mmol), and the mixture was stirred for 2.5 hrs at room temp. TBAF (0.112 mL, 0.112 mmol) was added and the mixture was stirred for 40 hrs at room temp. After addition of EtOAc the mixture was washed with water and brine, dried over Na2SO4 and evaporated to give an oily residue which was purified by Combiflash (12 g silica gel). Elution with 7:93 MeOH—CH2Cl2 gave a white solid residue which was repurified by prep HPLC to give 4-(5-(2-(1-(3,5-difluorophenyl)cyclohexyl)ethyl)-1,2,4-oxadiazol-3-yl)pyridin-2(1H)-one (4.8 mg, 16.64% yield) as a white solid. HPLC: tR=3.95 min, Waters Sunfire C18 4.6×50 mm, 4 min gradient, Detection Wave length 220 nm, Starting solvent: 10% aq. MeOH-0.1% TFA; Final solvent: 90% aq. MeOH-0.1% TFA. LC/MS: m/e 386.13 (M+H)+. 1H NMR (400 MHz, CDCl3): δ ppm 7.45 (1 H, d), 7.24 (1H, s), 6.84-6.88 (3 H, m), 6.65 (1H, m), 2.56-2.6 (2 H, m), 2.05-2.07 (4 H, m), 1.23-1.63 (8 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187437B2
Source datasetuspto-grants-2015_11
ORD IDord-76fa4ca7b0cc4657b1db25af7140bac6
Source noteuspto-grants-2015_11