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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864601Generated: October 26, 2026

Lithium borohydride → HCID 178418978, compound

https://huagongshe.com/reaction/1864601

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 (2 g, 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 numberUS07625913B2
Source datasetuspto-grants-2009_12
ORD IDord-c31d7942d4644c10a740ff000d3173b4
Source noteuspto-grants-2009_12