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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245076Generated: October 25, 2026

Water → 2-Chloro-4-[[(1S,2R)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrile

https://huagongshe.com/reaction/245076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant(1R,2S)-2-aminocyclohexan-1-ol hydrochlorideHCID 12228413—
Reactant2-Chloro-4-fluoro-3-methylbenzonitrileHCID 44550971—
SolventHydrochloric AcidHCID 313—
SolventDimethyl SulfoxideHCID 679—
Product2-Chloro-4-[[(1S,2R)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrileHCID 8669378568%

Reaction Steps

A solution of 2-chloro-4-fluoro-3-methyl-benzonitrile (500 mg, 2.95 mmol), (1R,2S)-2-aminocyclohexanol hydrochloride (671 mg, 4.42 mmol, Small Molecules, Inc.) and sodium bicarbonate (991 mg, 11.8 mmol) in DMSO (14.7 mL), and water (2.1 mL) is heated at 130° C. for 48 h. After cooling to room temperature, the mixture is diluted with 1 N HCl and extracted twice with EtOAc. The organic layers are combined, dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue is purified using radial chromatography, eluting with 2% methanol/dichloromethane to furnish the title compound as an off-white solid (527 mg, 68%). LC-ES/MS m/z 265.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658693B2
Source datasetuspto-grants-2014_02
ORD IDord-ec65236738ad4f70a18c4c5f6f6088e9
Source noteuspto-grants-2014_02