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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013903Generated: October 25, 2026

Lithium borohydride → HCID 178418978, compound

https://huagongshe.com/reaction/1013903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 178418985HCID 178418985—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178418978HCID 178418978—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of [6-methoxycarbonyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (2g, 4.85 mmol) in THF (100 mL) is added lithium borohydride (0.32 g, 14.5 mmol). The reaction mixture is stirred at 50° C. for 1.5 hours. The reaction is then quenched with dilute HCl and extracted with ethyl acetate. The organic layer is successively washed with aqueous saturated NaHCO3 and brine, dried over MgSO4 and evaporated. The solid residue is triturated in ethyl acetate and the resulting white solid is collected by filtration to give the desired product [6-hydroxymethyl-2-(4-propionylamino-phenyl-sulfanyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982037B2
Source datasetuspto-grants-2011_07
ORD IDord-1123abcfb99e41059ef0ed532555f23b
Source noteuspto-grants-2011_07