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HRID 704580Erstellt: 24. Oktober 2026

Aluminum;lithium;tetrachloride → (+/-)-6-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-4,5,6,7-tetrahydro-2-benzothiazolamine

https://huagongshe.com/de/reaction/704580

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAluminum;lithium;tetrachlorideHCID 166981—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt(+/-)-1-[(2-Amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-carbonyl]-1,2,3,6-tetrahydro-4-phenylpyridineHCID 15101105—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(+/-)-6-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-4,5,6,7-tetrahydro-2-benzothiazolamineHCID 15101109—

Reaktionsschritte

An ice-cold solution of aluminum chloride (0.80 g) in 20 ml of diethyl ether is added dropwise to a suspension of lithium aluminum chloride (0.65 g) in 30 ml of tetrahydrofuran and 30 ml of diethyl ether under nitrogen. The mixture is stirred at room temperature for 15 minutes and a solution of (±)-1-[(2-amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-carbonyl]-1,2,3,6-tetrahydro-4-phenylpyridine (3.5 g) (Example 6a) in 50 ml of tetrahydrofuran is added dropwise. The reaction mixture is stirred at 40° C. for 30 minutes. After cooling in an ice bath, the reaction is quenched by careful addition of 4 ml of a 10% solution of hydrochloric acid, 4 ml of a 30% solution of sodium hydroxide and 4 ml of water. The salts that precipitate are filtered through Celite and the filtrate evaporated and purified by MPLC (silica; 5% methanol, 95% dichloromethane). The title compound is obtained as a beige solid; mp 187° -190° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04988699
Quelldatensatzuspto-grants-1991_01
ORD IDord-151d200451404f31b9ba084a84df4a28
Quellennotizuspto-grants-1991_01