Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | HCID 57948923 | HCID 57948923 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57948943 | HCID 57948943 | 82% |
Reaction Steps
To a 0° C. solution of (S)-N-(2-(3-bromo-4-fluorophenyl)-4-methylpent-4-en-2-ylcarbamothioyl)benzamide (1.3 g, 3.0 mmoles, 1.0 equiv) in dichloromethane (40 mL) is added iodine (1.5 g, 5.9 mmoles, 2.0 equiv). The reaction is stirred at 0° C. for 1 h and gradually warmed to room temperature. The reaction mixture is quenched with saturated aqueous sodium thiosulfate. The aqueous layer is extracted with dichloromethane. The combined organic phase is dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (82% yield): MS (m/z): 561, 563 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648983B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-22c6fa7019ad43298b4a64a8007508f0 |
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| Source note | uspto-grants-2010_01 |
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