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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059375Generated: October 31, 2026

N-methyl-N-(trimethylsilyl)trifluoroacetamide → 1-(10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)-1-azoniabicyclo[2.2.2]octane-4-carboxylate

https://huagongshe.com/reaction/1059375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
Reactant8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazineHCID 11747038—
ReactantQuinuclidine-4-carboxylic acidHCID 13760939—
SolventAcetonitrileHCID 6342—
Product1-(10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)-1-azoniabicyclo[2.2.2]octane-4-carboxylateHCID 1867067714.3%

Reaction Steps

0.620 g of 1-azabicyclo[2.2.2]octane-4-carboxylic acid was dissolved in 40 ml of acetonitrile. After adding 3.98 g of N-methyl-N-(trimethylsilyl)trifluoroacetamide, the resulting mixture was stirred for 2 hours. Next, 0.998 g of 8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine was added thereto and the resulting mixture was heated under reflux for 4 hours. After distilling off the solvent under reduced pressure, the residue was dissolved in methanol/dichloromethane. After adding diethyl ether, the mixture was filtered and the residue was purified by High-porous gel chromatography (CHP20P, mfd by Mitsubishi Chemical Industries, 75-150μ) (eluted with methanol/water) to thereby give 0.21 g of the title compound as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-749fd764ca0d4a5ab2632083708a8b52
Source noteuspto-grants-2003_02