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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207427Generated: November 2, 2026

Methyl iodide → HCID 131735918, compound

https://huagongshe.com/reaction/2207427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 118093050HCID 118093050—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 131735918HCID 131735918—

Reaction Steps

A solution of ethyl 2,2-difluoro-3-hydroxy-3-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)pyridin-2-yl]propanoate (86.9 mg, 0.180 mmol), anhydrous DMF (1.00 mL), DBU (0.170 mL, 1.13 mmol) and CS2 (0.110 mL, 1.83 mmol) was stirred at room temperature for 1 hour under Ar(g). Methyliodide (0.110 mL, 1.76 mmol) was added to the reaction mixture and t stirred for 45 minutes at room temperature. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography (20% ethyl acetate in hexanes) to afford ethyl 2,2-difluoro-3-{[(methylsulfanyl)carbonothioyl]oxy}-3-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)pyridin-2-yl]propanoate. MS APCI C24H22F5N4O3S2 [M+H]+ 573. found 573.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376418B2
Source datasetuspto-grants-2016_06
ORD IDord-6f6b56e642e04fbea67db869347dc1c2
Source noteuspto-grants-2016_06