Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,1-Dimethylethyl N-[(phenylamino)sulfonyl]carbamate | HCID 405110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 90410761 | HCID 90410761 | 39% |
Reaction Steps
To a solution of tert-butyl N-phenylsulfamoylcarbamate (2.0 g, 7.35 mmol) and 1,4-dibromobutane (1.6 g, 7.35 mmol) in acetone (30 mL) was added Cs2CO3 (7.2 g, 22.05 mmol) and the mixture was stirred at 60° C. for 48 hours. The reaction mixture was filtered and concentrated under reduced pressure to afford tert-butyl 1,1-dioxo-7-phenyl-1λ6,2,7-thiadiazepane-2-carboxylate as a yellow oil (860 mg, 39%). LCMS (ESI): m/z=271.1 [M−56+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08912219B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-0e2031cd5a8b494e8fc84b89a205b7cb |
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| Source note | uspto-grants-2014_12 |
|---|