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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704580Generated: October 26, 2026

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

https://huagongshe.com/reaction/704580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum;lithium;tetrachlorideHCID 166981—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant(+/-)-1-[(2-Amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-carbonyl]-1,2,3,6-tetrahydro-4-phenylpyridineHCID 15101105—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-6-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-4,5,6,7-tetrahydro-2-benzothiazolamineHCID 15101109—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988699
Source datasetuspto-grants-1991_01
ORD IDord-151d200451404f31b9ba084a84df4a28
Source noteuspto-grants-1991_01