HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methyl-N-(trimethylsilyl)trifluoroacetamide → 1-(10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)-1-azoniabicyclo[2.2.2]octane-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-N-(trimethylsilyl)trifluoroacetamide | HCID 32510 | — |
| Reactant | 8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine | HCID 11747038 | — |
| Reactant | Quinuclidine-4-carboxylic acid | HCID 13760939 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)-1-azoniabicyclo[2.2.2]octane-4-carboxylate | HCID 18670677 | 14.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518423B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-749fd764ca0d4a5ab2632083708a8b52 |
| Source note | uspto-grants-2003_02 |