Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | (R)-5-Hydroxymethyltolterodine | HCID 9819382 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Fesoterodine | HCID 6918558 | — |
Reaction Steps
Drops of a solution of 18.6 g isobutyric acid chloride in 250 ml dichloromethane were added in approximately 10 minutes to a solution of 59.8 g (175.1 mol) (R)-2-[3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)phenol cooled to −3° C. (A, see FIG. 1) dissolved in 750 ml dichloromethane with agitation and cooling by ice bath. A white substance precipitated after approximately 5 minutes. For this purpose drops of a solution of 17.7 g triethylamine in 250 ml dichloromethane were added in 5 minutes under agitation and ice bath cooling. The batch was washed once with each of 250 ml water, 250 ml approximate 5% aqueous NaHCO3 solution and 250 ml water. The dichloromethane extract dried over Na2SO4 was evaporated to a low small bulk on a rotary evaporator to constant weight, whereby a pale yellow, high viscosity oil was left.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989654B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-7e581be49d7140eb82f06fb4839a9df1 |
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| Source note | uspto-grants-2011_08 |
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