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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Reactant | [3-(Aminomethyl)-3-hydroxy-1-azetidinyl][3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl]methanone | HCID 16222191 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67051949 | HCID 67051949 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915250B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-9a813bd7ad294862aca6fc308c180d10 |
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| Source note | uspto-grants-2011_03 |
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