Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | HCID 10132502 | HCID 10132502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22388583 | HCID 22388583 | 160.8% |
Reaction Steps
To a solution of {2-[4-(3-aminophenyl)phenoxy]propyl}[(methylethyl)sulfonyl]amine (145 mg, 0.416 mmol, prepared in example 3) dissolved in methylene chloride (2.8 mL, anhydrous), was added triethylamine (0.15 mL, 1.04 mmol) under a nitrogen system. The mixture was cooled to 0° C. and isobutyryl chloride (0.13 mL, 1.25 mmol) was added by syringe. The mixture was allowed to warm to room temperature, and stirred overnight, under a nitrogen system. The reaction was quenched with excess water, and the organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced vacuum, yielding 280 mg viscous oil. Purification was conducted using a Chromatotron®, on a 4000 μm rotor and eluting with a 1:1 hexane:ethyl acetate solvent system, yielding the title compound (136 mg, 78%) as a slow crystallizing foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06911476B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-be1ccf8ae0e4424a9718b8627447858e |
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| Source note | uspto-grants-2005_06 |
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