Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25502Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/25502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamineHCID 9943439—
SolventDichloromethaneHCID 6344—
Product[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4-methoxy-benzyl)-amineHCID 1029402746.3%

Reaction Steps

4-Methoxybenzaldehyde (0.204 g, 1.5 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.405 g, 1.48 mmol) in methylene chloride (125 mL), followed by acetic acid (0.3 g, 1.5 mmol). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.31 g, 1.46 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 3 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 yellow oil. Recrystallization from methanol/water gave the product as off-white crystals (270 mg); mp 173-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858739B2
Source datasetuspto-grants-2005_02
ORD IDord-5446955f4f5346a18a8e2ea598f19e1b
Source noteuspto-grants-2005_02