Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | HCID 178467255 | HCID 178467255 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57999028 | HCID 57999028 | 24% |
Reaction Steps
To a 150 mL pressure vessel was added 5-(2-bromo-4-fluorophenyl)-2-(1-hydroxyethylidene)cyclohexane-1,3-dione (1E, 1.12 g, 3.42 mmol, 1.0 eq.), EtOH (30 mL), guanidine hydrochloride (818 mg, 8.56 mmol, 2.5 eq.), and dimethylamine (2.0 M in THF, 10 mL, 20.5 mmol, 6.0 eq.). The vessel was sealed and heated for 72 hours at 100° C. LC/MS determined the reaction to be complete. The reaction was cooled and concentrated to give a pasty gray solid. EtOH (˜10 mL) was added to the residue and sonicated to give a suspension. The solid was collected by filtration and rinsed with cold EtOH to give a light-yellow solid (288 mg, 24%). ESI-MS: m/z 350.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071766B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-f461fdb07e1d4bb8a07efd08274632ca |
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| Source note | uspto-grants-2011_12 |
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