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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539647Generated: November 1, 2026

Sodium borohydride → HCID 58200236, compound

https://huagongshe.com/reaction/539647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58200290HCID 58200290—
SolventTrifluoroacetic acidHCID 6422—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58200236HCID 5820023611.3%

Reaction Steps

To a stirring suspension of (2-bromo-4,5-dimethoxy-phenyl)-(5-phenyl-[1,2,4]triazolo[4,3-a]pyrazin-3-yl)-amine (0.2 g, 3.7 mmol) in a mixture of THF (20 mL) and TFA (1 mL) at 0° C. was added sodium borohydride (20 mg, 4.0 mmol). The reaction mixture was stirred 15 minutes at room temperature, thane quenched by addition of 10% aqueous HCl. The resulting mixture was heated to reflux for 10 minutes, then cooled and made basic by addition of 1M aqueous NaOH. The mixture was extracted with EtOAc, and the combined organic layers were dried (MgSO4), filtered and concentrated under reduced pressure to give 0.18 g of (2-bromo-4,5-dimethoxy-phenyl)-(5-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazin-3-yl)-amine, MS (M+H)=431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871760B2
Source datasetuspto-grants-2014_10
ORD IDord-a14f3c02db594a4e8949614ac37b781a
Source noteuspto-grants-2014_10