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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74940Generated: October 29, 2026

Ethyl Acetate → (3S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanol

https://huagongshe.com/reaction/74940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant(S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)cyclohexanoneHCID 86667417—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product(3S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanolHCID 86667419—

Reaction Steps

To a solution of (3S)-3-[(2-chloro-5-fluoro-pyrimidin-4-yl)amino]cyclohexanone (1.83 g, 7.49 mmol) in THF (100 mL) was added methylmagnesium bromide (21.4 ml of 1.4M solution, 29.96 mmol) at room temperature. The reaction mixture was stirred at room temperature for 5 minutes. To the reaction mixture was added aqueous saturated NH4Cl solution and EtOAc. The organic phase was washed with brine and dried with MgSO4, filtered and concentrated in vacuo. The two spots were separated by silica gel chromatography (120 g silica gel column).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829007B2
Source datasetuspto-grants-2014_09
ORD IDord-f6694c669f1f40aa967a6ec15e78555d
Source noteuspto-grants-2014_09