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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1950275Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1950275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt4-(2-(Piperidin-1-yl)ethoxy)benzaldehydeHCID 11183892—
Edukt5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenylamineHCID 23087522—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[5-Methoxy-2-(6-methoxybenzothiazol-2-yl)phenyl][4-(2-piperidin-1-ylethoxy)benzyl]amineHCID 5793379015,9%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399520B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-5018dcfbc7d446afbd488243532fd30a
Quellennotizuspto-grants-2013_03