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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296307Generated: November 2, 2026

Methyl iodide → HCID 58911620, compound

https://huagongshe.com/reaction/1296307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 58911555HCID 58911555—
SolventDimethylformamideHCID 6228—
ProductHCID 58911620HCID 5891162079%

Reaction Steps

To a solution of the title compound of Example 215 (23.0 mg, 0.0965 mmol) in dimethylformamide (0.75 mL) were added cesium carbonate (94 mg, 0.29 mmol) and methyl iodide (0.0072 mL, 0.12 mmol). After 4.5 h, the reaction was partitioned between dichloromethane (2 mL) and water (2 mL). The aqueous layer was extracted with dichloromethane (2 mL). The combined organic layers were dried (sodium sulfate) and concentrated in vacuo. The residue was taken up in a minimum amount of 50% aqueous methanol and loaded onto a methanol-activated water-equilibrated 1-g SCX-type cation exchange column. The column was washed with water (6 mL) and 50% aqueous methanol (6 mL). The column was eluted with 2N methanolic ammonia (8 mL). This fraction was concentrated in vacuo to provide (−)-1,2,3,4,11,11a-hexahydro-2-methyl-pyrazino[1,2-b][1,2]benzothiazine 6,6-dioxide as a white solid (19 mg, 79%): LCMS (pos. ion spectrum) m/z 253.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244843B2
Source datasetuspto-grants-2007_07
ORD IDord-49d7b9c8a06f44f883f06cceecd695cb
Source noteuspto-grants-2007_07