Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (s)-Tert-butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide | HCID 11195739 | — |
| Reactant | HCID 178422359 | HCID 178422359 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131724706 | HCID 131724706 | — |
Reaction Steps
To a solution of 0.95 g 5-bromo-2-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxymethyl]-6-methyl-1H-indole in 10 mL N,N-dimethylformamide was added 0.143 g sodium hydride (55-65%, mineral oil) and the mixture was stirred 30 min at room temperature. To the resulting mixture was added (S)-5-methyl-2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester (0.703 g) and the mixture was stirred 2 h at room temperature. The reaction mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase was washed with 10% citric acid and brine, dried over magnesium sulfate and purified by chromatography on silica gel with 5:1 hexane:ethyl acetateto yield 0.789 g of the title compound as a slightly yellow oil. MS: M+H=541.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06844345B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-6ccc3929069545e68cafff540db6624a |
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| Source note | uspto-grants-2005_01 |
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