Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 4,5-Dichloro-1,2-phenylenediamine | HCID 79297 | — |
| Reactant | 4-Cyclohexylbenzenamine | HCID 80764 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69417851 | HCID 69417851 | — |
Reaction Steps
To a stirring solution of 4-cyclohexylaniline (10 mmol, 1.75 g) and DIEA (21 mmol, 3.65 mL) in CH2Cl2 (10 mL) at 0° C. was added thiophosgene (10 mmol, 700 μL) dropwise. The solution was allowed to reach ambient temperature for 1 h, and 4,5-dichloro-1,2-phenylenediamine (10.5 mmol, 1.86 g) was added. The reaction mixture was heated to reflux for 2 h, then concentrated in vacuo. The residue was taken up in a solution of EtOH (5 mL) and MeI (20 mmol, 1.25 muL), heated at 40° C. for 16 h, and concentrated in vacuo. Flash chromatography on silica eluting with 18-25% EtOAc in hexanes afforded the product as a red solid. LC-MS (ESI, Method C): 3.47 min, m/z 360.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07301036B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-dd0ade8574f449aeb83b7831f5c6edfe |
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| Source note | uspto-grants-2007_11 |
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