Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | 4-Cyano-1H-imidazole-2-carboxylic acid [4-bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenyl]-amide | HCID 178424443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58994583 | HCID 58994583 | 50% |
Reaction Steps
To a suspension of 4-cyano-1H-imidazole-2-carboxylic acid [4-bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenyl]-amide (71 mg, 0.18 mmol) (as prepared in Example 14, step (c)) in 3 mL THF at −40° C. was added a 2M solution of isopropylmagnesium chloride (i-PrMgCl) in THF (0.23 mL, 0.46 mmol) and the solution was then warmed to 0° C. and stirred for 10 min. The solution was then cooled to −78° C. and a 1.7 M solution of t-BuLi in pentane (0.28 mL, 0.48 mmol) was added dropwise and then a 40% solution of ethyl glyoxalate in toluene (0.23 mL, 0.90 mmol) was added immediately thereafter. After 5 min at −78° C. the reaction was quenched with satd NH4Cl (10 mL) and extracted with EtOAc (3×10 mL) and dried over Na2SO4 and concentrated in vacuo. The title compound was purified by flash chromatography (silica gel) eluting with 50-100% EtOAc/hexanes to give 37 mg (50%) of the title compound as a white solid. Mass spectrum (ESI, m/z): Calcd. for C23H26N4O2, 423.2 (M+H). found 423.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674100B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-eba688ae218e4f4ba9585b5877e36433 |
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| Source note | uspto-grants-2014_03 |
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