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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133602Generated: October 27, 2026

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

https://huagongshe.com/reaction/133602

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

A 5% acetic acid/methanol (1.0 mL) solution of 4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine (20.0 mg, 0.058 mm ol) and 3-hydroxy-4-methoxybenzaldehyde (33 mg) was added to a 5% acetic acid/methanol (1.0 mL) solution of NaBH3CN (16.5 mg), and the mixture was stirred at 60° C. for 15 hours. The resulting reaction mixture wa's then loaded onto a Varian™ SCX column and washed with methanol (15 mL). The obtained crude product was eluted with a 2 M NH3-methanol (5 mL) and concentrated to thereby afford 1-[3-hydroxy-4-methoxybenzyl]4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine (Comp d. No. 1452) (25.8 mg, 92%). The purity was determined by RPLC/MS (91%). ESI/MS m/e 480 (M++H, C24H28F3N3O4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-45c55b9155c04d7f88334d4703b0d321
Source noteuspto-grants-2008_06