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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827279Generated: November 1, 2026

1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → HCID 12150153, compound

https://huagongshe.com/reaction/1827279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(1,3-Thiazol-2-yl)benzaldehydeHCID 15532482—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 12150153HCID 12150153—

Reaction Steps

To a mixture of 2-(2-thiazolyl)benzaldehyde (200 mg, 1.06 mmol) and 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (0.232 mg, 1.00 mmol) in 1,2-dichloroethane (20 mL) was added sodium triacetoxyborohydride (376 mg, 1.79 mmol). The resultant mixture was stirred at room temperature for 18 h, quenched with aqueous NaHCO3 (50 mL) and extracted with CHCl3 (2×50 mL). The organic solution was dried over Na2SO4, filtered and concentrated. The crude product was dissolved in 1:1 CHCl3:CH3OH (30 mL) and treated with 2 mL of 1N HCl in Et2O. The HCl salt was precipitated by addition of Et2O, collected by filtration and dried in the vacuum oven at 60° C. for 18 h to yield the product as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053101B2
Source datasetuspto-grants-2006_05
ORD IDord-e24fe329fe8b4bf0b65bb1f8b950ea6c
Source noteuspto-grants-2006_05