Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tert-butyl 3-((methanesulfonyloxy)methyl)azetidine-1-carboxylate | HCID 21959416 | — |
| Reactant | 7-Methoxy-1,2-dihydroquinolin-2-one | HCID 29942756 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67130938 | HCID 67130938 | 44% |
Reaction Steps
A suspension of 7-methoxy-2(1H)-quinolinone (405 mg; commercial) in DMF (10 mL) was treated with NaH (111 mg; 50% dispersion in oil). The mixture was stirred at rt for 30 min before the addition of a solution of 3-[[(methylsulfonyl)oxy]methyl]-1-azetidinecarboxylic acid tert-butyl ester (674 mg; prepared according to WO 02/066470) in DMF (2 mL). The mixture was heated at 100° C. overnight. The reaction mixture was partitioned between EA and water. The org. phase was dried over MgSO4, concentrated under reduced pressure and purified by CC (Hept/EA 2:1 to 0:1). The second eluting compound was isolated as a colourless foam (350 mg, 44% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507478B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c769a287126248d1b7a108a116885929 |
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| Source note | uspto-grants-2013_08 |
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