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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198437Generated: October 26, 2026

N,N-Dimethylaniline → 2-(4-chlorophenyl)-4-(dimethylamino)acetyl-3,4-dihydro-2H-1,4-benzothiazine hydrochloride

https://huagongshe.com/reaction/1198437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-chlorophenyl)-3,4-dihydro2H-1,4-benzothiazineHCID 13071524—
Reactant2-(Dimethylamino)acetyl chloride hydrochlorideHCID 13994991—
SolventDichloromethaneHCID 6344—
Product2-(4-chlorophenyl)-4-(dimethylamino)acetyl-3,4-dihydro-2H-1,4-benzothiazine hydrochlorideHCID 19794236165.5%

Reaction Steps

To a solution of 2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (0.52 g) ad N,N-dimethylaniline (0.97 g) in methylene chloride (15 ml) is added dimethylaminoacetyl chloride hydrochloride (0.63 g) under ice cooling, and the mixture is stirred at the same temperature for 2.5 hours. To the reaction mixture is added aqueous sodium hydrogen carbonate solution, and is extracted with chloroform. The chloroform layer is washed, dried and distilled to remove the solvent. The residue is treated with hydrochloric acid and the resulting salt is recrystallized from ethanol-ether to give 2-(4-chlorophenyl)-4-(dimethylamino)acetyl-3,4-dihyro-2H-1,4-benzothiazine hydrochloride (0.63 g, yield 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281592
Source datasetuspto-grants-1994_01
ORD IDord-6f0ea970d22f4f9b96f624c3d8130e1f
Source noteuspto-grants-1994_01