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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423845Generated: October 26, 2026

Ammonia → [5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenyl][4-(2-piperidin-1-ylethoxy)benzyl]amine

https://huagongshe.com/reaction/2423845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-(2-(Piperidin-1-yl)ethoxy)benzaldehydeHCID 11183892—
Reactant5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenylamineHCID 23087522—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product[5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenyl][4-(2-piperidin-1-ylethoxy)benzyl]amineHCID 5793379015.9%

Reaction Steps

To a suspension of 5-methoxy-2-(6-methoxybenzothiazol-2-yl)phenylamine (473 mg) and 4-(2-piperidin-1-ylethoxy)benzaldehyde (484 mg) in tetrahydrofuran (6 ml), dichloromethane (4 ml) and acetic acid (4 ml) was added borane-methyl sulfide complex (0.18 ml), and the solution was stirred for 6 hours at room temperature. The solution was neutralized with ammonia solution on an ice bath, extracted with ethyl acetate, then sequentially washed with water and brine, and the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (132 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-963b8805149b4479a0d07f6822233743
Source noteuspto-grants-2011_06