Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | HCID 66873657 | HCID 66873657 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 66873722 | HCID 66873722 | — |
Reaction Steps
To a solution of methyl 2-((2S,6S)-2,6-dimethyl-4-(piperidine-1-carbonyl)piperazin-1-yl)benzoxazole-4-carboxylate (200 mg, 0.52 mmol) in pyridine (2 mL) was added lithium iodide (495 mg, 3.70 mmol). The mixture was heated at 110° C. for 18 h and allowed to cool to ambient temperature before partitioning with 9:1 dichloromethane/2-propanol (100 mL) and 1 N HCl (50 mL). The non-homogenous organic layer was washed with brine and concentrated in vacuo. The residue was treated with 9:1 mixture of toluene and methanol (100 mL) and concentrated under reduced pressure to afford crude 2-((2S,6S)-2,6-dimethyl-4-(piperidine-1-carbonyl)piperazin-1-yl)benzoxazole-4-carboxylic acid as a brown solid which was directly elaborated without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863271B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-420f2568c4ca42d8a3d0a3754fb39e52 |
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| Source note | uspto-grants-2011_01 |
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