Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Bromide | HCID 6323 | — |
| Reactant | Tolterodine | HCID 443879 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 9953901 | HCID 9953901 | — |
Reaction Steps
A sealed mixture of methyl bromide (100 g) and 2-[(1R)-3-(diisopropylamino)-1-phenylpropyl]-4-methylphenol (14 g) in acetone (100 ml) is stirred at 20-25° C. for 4 days. The mixture is cooled to −10° C. and the precipitate is filtered off and washed with ether and dried to give the title compound, mp 189-191° C. (dec). Anal Calcd for C23H34BrNO: C, 65.71; H, 8.15; Br, 19.00; N, 3.33. Found: C, 65.61; H, 8.34; Br, 19.12; N, 3.32. [α]D (c=1, MeOH) +25° C. 1H NMR [(CD3)2SO] δ 1.25, 2.18, 2.48, 2.81, 3.05, 3.89, 4.22, 6.70, 6.83, 7.08, 7.19, 7.33, and 9.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439397B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-5dfc899a0dc34adcbc5c86a4053b9210 |
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| Source note | uspto-grants-2008_10 |
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