Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25501Generated: October 25, 2026

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

https://huagongshe.com/reaction/25501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-ThiophenecarboxaldehydeHCID 7364—
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]-thiophen-2-ylmethyl-amineHCID 994755732.4%

Reaction Steps

2-Thiophenecarboxaldehyde (0.112 g, 1.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.29 g, 1.06 mmol) in methylene chloride (125 mL), followed by acetic acid (0.1 g, 1.67 mmol). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.23 g, 1.09 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 6 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken and the organic layer separated. The solvent was evaporated to give a brown gum. Recrystallization from methanol/water gave the product as a brown solid (120 mg), mp 190-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858739B2
Source datasetuspto-grants-2005_02
ORD IDord-adbbe9c4bdb14caca4ed935cc7bb7baf
Source noteuspto-grants-2005_02