Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86640018 | HCID 86640018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86640019 | HCID 86640019 | — |
Reaction Steps
A mixture of give 1-(3′-methylsulfonyl)biphenyl-4-yl)-2-(2-(trifluoromethyl)phenyl-1H-imidazole-4-carbonitrile (694 mg, 1.485 mmol), NH2OH.HCl (258 mg, 3.71 mmol), Et3N (0.6 mL, 4.3 mmol), and dry EtOH (15 mL) was stirred at 55° C. for 5 h under N2. The solvent was removed in vacuo to give N′-hydroxy-1-(3′-methylsulfonyl)biphenyl-4-yl)-2-(2-(trifluoromethyl)phenyl-1H-imidazole-4-carboximidamide as a white solid, which was used in the next reaction without further purification. MS (ESI) 501 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998995B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-3a8393e1935349a0b1e0040d5913ecaf |
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| Source note | uspto-grants-2011_08 |
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