Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10615554 | HCID 10615554 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10624052 | HCID 10624052 | 34% |
Reaction Steps
A solution of [[[2,6-bis(1-methylethyl)phenyl]-amino]carbonyl]sulfamoyl chloride (1.0 g, 3.1 mmoles) in 60 mL Et2O was added dropwise to a solution of benzhydrylamine (0.56 g, 3.1 mmoles) and 0.5 mL triethylamine (3.4 mmoles) in 60 mL Et2O at -15° C. (acetone/ice bath) under an atmosphere of N2. The resulting suspension was warmed to 25° C. and stirred for 16 hours. This was then partitioned between 1N HCl and EtOAc. The EtOAc layer was dried with MgSO4, filtered, and evaporated to give an off-white solid. Chromatography (SiO2, 30% EtOAc/hexanes) gave 0.49 g (34%) of the title compound as a white solid, mp 182°-185° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05288757 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-4e95a1bd522d46ec9bff5493bcd69ae2 |
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| Source note | uspto-grants-1994_02 |
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