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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279315Generated: November 1, 2026

Isovanillin → 1-(3-hydroxy-4-methoxybenzyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine

https://huagongshe.com/reaction/279315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsovanillinHCID 12127—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-[{N-(3(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidineHCID 18426164—
SolventAcetic acid methanolHCID 10129899—
Product1-(3-hydroxy-4-methoxybenzyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidineHCID 18426263—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (20.0 mg, 0.058 mmol) and 3-hydroxy-4-methoxybenzaldehyde (33 mg) in 5% CH3COOH/CH3OH (1.0 mL) was added NaBH3CN (16.5 mg) in 5% CH3COOH/CH3OH (1.0 mL). The reaction mixture was stirred at 60° C. for 15 h. The reaction mixture was loaded onto Variant™ SCX column and washed with CH3OH (15 mL). Product was eluted using 2 N NH3-CH3OH (5 mL) and the eluant was concentrated to afford 1-(3-hydroxy-4-methoxybenzyl)-4-[{N-(3-(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (Compound No. 1452) (25.8 mg, 92%): The purity was determined by RPLC/MS (91%); ESI/MSm/e 480 (M++H, C24H28F3N3O4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-b8c0f279c7874b01be9da2e7eafd4e35
Source noteuspto-grants-2002_03