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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605740Generated: October 30, 2026

1,1-Bis(methylthio)-2-nitroethylene → HCID 67051949, compound

https://huagongshe.com/reaction/605740

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Bis(methylthio)-2-nitroethyleneHCID 83623—
Reactant[3-(Aminomethyl)-3-hydroxy-1-azetidinyl][3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl]methanoneHCID 16222191—
SolventEthanolHCID 702—
ProductHCID 67051949HCID 6705194939%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-(aminomethyl)-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-ol (0.24 g, 0.5 mmol), prepared using procedures similar to those described in Example 3, and commercially available 1,1-bis(methylthio)-2-nitroethylene (0.083 g, 0.5 mmol) in ethanol (5 mL) was stirred at 70° C. for 16 hours. The reaction mixture was concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated to afford 0.10 g, (39%) 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-3-({[(Z)-1-(methylthio)-2-nitroethenyl]amino}methyl)azetidin-3-ol. MS (EI) for C20H18F3IN4O4S: 595 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915250B2
Source datasetuspto-grants-2011_03
ORD IDord-9a813bd7ad294862aca6fc308c180d10
Source noteuspto-grants-2011_03