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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434087Generated: October 26, 2026

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

https://huagongshe.com/reaction/1434087

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 numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-f977de0866114ecd8ed47ea8991849dd
Source noteuspto-grants-2009_11