HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486480Generated: October 25, 2026
2-Methylpyrazine → HCID 54206036, compound
https://huagongshe.com/reaction/486480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylpyrazine | HCID 7976 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-oxo-2-phenylacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester | HCID 22850700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54206036 | HCID 54206036 | — |
Reaction Steps
2-Methylpyrazine (0.94 g) in tetrahydrofuran (THF) (5 ml) was added dropwise to lithium diisopropylamide (LDA) (7.51 ml of a 1.5 molar solution in THF) in THF (20 ml) at -78° C. After 0.75 hour a solution of (R)-3-quinuclidinyl 2-phenylglyoxalate (see Preparation 2) (2.59 g) in THF (20 ml) was added, the reaction mixture was allowed to reach room temperature, stirred for 1 hour and partitioned between ethyl acetate and 10% aqueous potassium carbonate. The organic layer was then dried over magnesium sulphate and evaporated to leave a residue which was purified by chromatography on silica gel performing a gradient elution using chloroform plus methanol (0→15%). Appropriate fractions were combined and evaporated to give the title compound, as a yellow oil (1.4 g, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292749 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-4d2a6e14c26f4d4594f72d9e9719aae0 |
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| Source note | uspto-grants-1994_03 |
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