Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | HCID 28413999 | HCID 28413999 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 87103646 | HCID 87103646 | 40.8% |
Reaction Steps
To a solution of 0.988 ml 2,2,6,6-tetramethylpiperidine in 10 ml tetrahydrofurane was added 3.534 ml of a 1.6M solution of n-butyl lithium in hexane at ambient temperature and the mixture was stirred at room temperature for 30 min. To this solution was added rapidly a precooled (−75° C.) solution of 0.300 g 3-chloro-6-cyclopropylmethoxy-pyridazine in 10 ml tetrahydrofuran at −75° C. After 5 minutes, a precooled solution of 0.701 g iodine in 10 ml THF was added rapidly. The reaction mixture was stirred at −75° C. for 30 minutes and then quenched with a saturated aqueous solution of ammonium chloride and diluted with ethyl acetate. The phases were separated and the organic phase was purified by chromatography on silica gel using a gradient of heptane:ethyl acetate=95:5 to 50:50 to yield 0.206 g of the title compound as light yellow solid. MS (EI): 310.9 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669254B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-cdd1f7b7093243c1acff1f5937f778ca |
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| Source note | uspto-grants-2014_03 |
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