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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25531Generated: October 25, 2026

4-Cyanobenzaldehyde → [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4-cyano-benzyl)-amine

https://huagongshe.com/reaction/25531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamineHCID 9943439—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4-cyano-benzyl)-amineHCID 1013490738.5%

Reaction Steps

4-Cyanobenzaldehyde (0.262 g, 2.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.548 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.46 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 4 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken, the organic layer separated and dried over Na2SO4. The solvent was evaporated to give a colorless gum. Recrystallization from methanol gave the product (300 mg), mp 158-159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858739B2
Source datasetuspto-grants-2005_02
ORD IDord-c05e6a3daa3f4af4b7bf7e05025b41f0
Source noteuspto-grants-2005_02