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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480612Generated: October 26, 2026

Lithium borohydride → HCID 178418978, compound

https://huagongshe.com/reaction/480612

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 numberUS06653300B2
Source datasetuspto-grants-2003_11
ORD IDord-60fd620359364511ada02a06302f4139
Source noteuspto-grants-2003_11