Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | HCID 66874035 | HCID 66874035 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 66874469 | HCID 66874469 | — |
Reaction Steps
To a solution of methyl 2-((2S,6S)-2,6-dimethyl-4-(dimethylcarbamoyl)piperazin-1-yl)benzoxazole-4-carboxylate (265 mg, 0.74 mmol) in pyridine (5 mL) was added LiI (984 mg, 7.35 mmol). The mixture was heated at 110° C. for 14 h and allowed to cool to ambient temperature. The reaction was partially concentrated under reduced pressure before partitioning with 9:1 CH2Cl2/2-propanol (50 mL) and 1 N HCl (20 mL). The organic layer was washed with brine, dried (Na2SO4) and concentrated under reduced pressure to afford crude 2-((2S,6S)-2,6-dimethyl-4-(dimethylcarbamoyl)piperazin-1-yl)benzoxazole-4-carboxylic acid as an orange oil 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-c5e1c6a93d9f426da840db2658819d89 |
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| Source note | uspto-grants-2011_01 |
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