Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(3-Amino-4-methoxyphenyl)-N-cyclohexyl-N-methyl-1H-imidazole-1-carboxamide | HCID 66681874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66682452 | HCID 66682452 | 34% |
Reaction Steps
Mesyl chloride (0.247 mL, 3.17 mmol) was added to a stirred solution of 4-(3-amino-4-methoxyphenyl)-N-cyclohexyl-N-methyl-1H-imidazole-1-carboxamide (1.04 g, 3.17 mmol) and triethylamine (0.441 mL, 3.17 mmol) in tetrahydrofuran (6 mL) at room temperature. The brown mixture was allowed to stir at room temperature over the weekend. Water was added and the solvent was evaporated. Then the aqueous layer was acidified and the residue was extracted with ethyl acetate. The aqueous layer was extracted twice with a mixture of dichloromethane/isopropanol (7:3). The organic layer was separated, dried (MgSO4) filtered and evaporated to give an off-white solid. The solid was recrystallised from an ethanol/dichloromethane mixture to give the product as an off-white solid (434 mg, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353082B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-2cb286f14c82435fa80e788cb36ff421 |
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| Source note | uspto-grants-2016_05 |
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