Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 24748418 | HCID 24748418 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 101603487 | HCID 101603487 | — |
Reaction Steps
Cis- or trans- N,N-diethylhydroxytamoxifen (II) (100 mg, 0.27 mmol) was dissolved in methylene chloride (2 ml) and cooled to 0° C. Pyridine (150 μl) and tosyl chloride (55 mg, 0.27 mmol) were added. After 2 hours, the reaction mixture was diluted with methylene chloride and washed with water. The methylene chloride layer was evaporated and chromatographed on a 18C column using 85:15:1 acetonitrile/water/triethylamine as eluant to yield cis (51 mg, 34%, oil) or trans tosyl analog (30 mg, 20%, oil): m/z 569(60, M+), 397(20, +OSO2PhCH3). Values for aliphatic protons are presented in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096874 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-7ae97f0cdfbb4d22bc88d5f8c8972b06 |
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| Source note | uspto-grants-2000_08 |
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