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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081555Generated: November 1, 2026

Triethylamine → 6-chloro-4-methyl-N-(3-quinuclidinyl)-3,4-dihydro-2H-1,4-benzothiazine-8-carboxamide

https://huagongshe.com/reaction/2081555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant3-AminoquinuclidineHCID 123238—
Reactant6-chloro-4-methyl-3,4-dihydro-2H-1,4-benzothiazine-8-carboxylic acidHCID 10847851—
SolventEthyl AcetateHCID 8857—
Product6-chloro-4-methyl-N-(3-quinuclidinyl)-3,4-dihydro-2H-1,4-benzothiazine-8-carboxamideHCID 10498161—

Reaction Steps

To a solution of 1.8 g of 6-chloro-4-methyl-3,4-dihydro-2H-1,4-benzothiazine-8-carboxylic acid in 30 ml of ethyl acetate was added 1.05 g of triethylamine, and then added 0.891 g of pivaloyl chloride dropwise with stirring at -10° C. to -5° C. followed by stirring the mixture at the same temperature for 30 minutes. To the resultant mixture was added a solution of 1.12 g of 3-aminoquinuclidine in 15 ml of ethyl acetate at -10° to -5° C. and then stirred at room temperature for an hour. After the reaction solution was washed with water, dried over anhydrous sodium sulfate and concentrated, the crystalline residue thus obtained was recrystallized from ethyl acetate to give 6-chloro-4-methyl-N-(3-quinuclidinyl)-3,4-dihydro-2H-1,4-benzothiazine-8-carboxamide as yellow crystals. Melting point: 195°-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185333
Source datasetuspto-grants-1993_02
ORD IDord-23bbd03679e34015a1a68ac0b8217dff
Source noteuspto-grants-1993_02