Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | 5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridine | HCID 59218620 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178436275 | HCID 178436275 | 40% |
Reaction Steps
To a stirred solution of 5-[1-(methylthio)ethyl]-2-(trichloromethyl)-pyridine (B) (0.55 g, 2.3 mmol) and cyanamide (0.097 g, 2.3 mmol) in THF (7 mL) cooled to 0° C. was added iodobenzene diacetate (0.75 g, 2.3 mmol) in one portion. The resulting mixture was stirred at 0° C. for 1 hr and then at room temperature for 2 hr. The solvent was removed in vacuo and the resulting mixture was purified on silica gel using 50% acetone in hexane to give 0.254 g of (1E)-methyl {1-[6-(trichloromethyl)pyridin-3-yl]ethyl}-λ4-sulfanylidenecyanamide (C) as an off-white solid in 40% yield. 1H NMR for the diastereomeric mixture (300 MHz, d6-acetone) δ 8.87 (s, 1H), 8.21-8.25 (m, 2H), 4.65-4.76 (m, 1H), 2.86-2.66 (m, 3H), 1.88-1.92 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193364B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-59f4ff569add4922bc0dcd13b8df5609 |
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| Source note | uspto-grants-2012_06 |
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