Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743080Generated: October 30, 2026

3-Thiophenecarboxaldehyde → HCID 19423540, compound

https://huagongshe.com/reaction/743080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ThiophenecarboxaldehydeHCID 68135—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 19423601HCID 19423601—
ReactantEthanol hydrochlorideHCID 21887872—
SolventMethanolHCID 887—
ProductHCID 19423540HCID 1942354084%

Reaction Steps

To a solution of 500 mg (1.62 mmol) of 3-(piperidin-4-yl)-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrido[4,3-d]pyrimidine in 30 mL of methanol were added 1,200 mg of 10% HCl/ethanol solution, 727 mg (6.48 mmol) of 3-thiophenecarboxaldehyde and 407 mg (6.48 mmol) of sodium cyanoborohydride under ice-cooling, and the mixture was stirred for 10 hours at ambient temperature. Then, the reaction mixture was concentrated in vacuo, and water was added to the residue. The mixture was adjusted to pH 10 and extracted with chloroform. The organic layer separated was dried on potassium carbonate, and then concentrated in vacuo. The residue was purified by means of column chromatography (silica gel, 1:9 methanol:chloroform) to give 550 mg (1.36 mmol) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556860
Source datasetuspto-grants-1996_09
ORD IDord-8cb4df1b4eec469592f85fb925a0f28c
Source noteuspto-grants-1996_09