Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | HCID 22024483 | HCID 22024483 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22024372 | HCID 22024372 | — |
Reaction Steps
Ethyl bromoacetate (18.5 mL) and iso-dipropylethylamine (29 mL) were added to a solution of methyl N-(3-methoxy-2-pyrazinyl)-(methylsulfanyl)methaneimidothioate (19.1 g) in acetonitrile (42 mL), and the mixture was heated under stirring at 100° C. for 14 hours. After the reaction mixture was cooled to room temperature, water was added thereto, which was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate, and evaporated. The resulting residue was washed with n-hexane to give the title compound (10.7 g) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772249B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ce116dbef7034760b5f8d66e9bf1c63a |
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| Source note | uspto-grants-2010_08 |
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