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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503784Generated: November 3, 2026

Triethylamine → HCID 178432377, compound

https://huagongshe.com/reaction/503784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(2-Methyl-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)benzaldehydeHCID 86630681—
ReactantHCID 178478299HCID 178478299—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 178432377HCID 178432377—

Reaction Steps

0.25 ml triethylamine is added to a solution of 225 mg 4-(5-thiazol-2-yl-1H-[1,2,4]triazol-3-yl)-piperidine hydrochloride in 7.6 ml methanol. To this solution a solution of 250 mg 4-(2-methyl-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)benzaldehyde (prepared as described under example 37) in 7.6 ml DMF is added, followed by 0.11 ml glacial acetic acid and 337 mg NaBH(OAc)3. The resulting mixture is stirred at room temperature. Six additional portions of 2 equivalents NaBH(OAc)3 are added over 3 days. The solvent is removed by evaporation and the residue is purified by chromatography on silica gel (dichloromethane/[dichloromethane+7M NH3 in methanol]) to yield the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776864B2
Source datasetuspto-grants-2010_08
ORD IDord-68e3e070fc4648a9ae9c8e5d7e23ec35
Source noteuspto-grants-2010_08