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2,5-Disubstituted Bicyclo[2.1.1]hexanes as Rigidified Cyclopentane Variants for Medicinal Chemistry
Shashwati Paul ; Daniel Adelfinsky ; Christophe Salome , et al. Chem. Sci.,2023,14(30):8070-8075. DOI: 10.1039/D3SC02695G
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Abstract: Identification of rigid counterparts for common flexible scaffolds is crucial to the advancement of medicinal chemistry. Here we showcase a new class of building blocks, 2,5-disubstituted bicyclo[2.1.1]hexanes that can act as rigidified cis-, or trans-1,3-disubstituted cyclopentanes, common motifs in drugs. The scalable synthesis of these structures was enabled through the use of C–H functionalization logic and cycloaddition reactions.
CAS No. : | 1779-49-3 | MDL No. : | MFCD00011804 |
Formula : | C19H18BrP | Boiling Point : | - |
Linear Structure Formula : | CH3(C6H5)3PBr | InChI Key : | LSEFCHWGJNHZNT-UHFFFAOYSA-M |
M.W : | 357.22 | Pubchem ID : | 74505 |
Synonyms : |
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Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P261-P264-P270-P271-P301+P310-P304+P340-P312-P330-P403+P233-P405-P501 | UN#: | 2811 |
Hazard Statements: | H301-H411 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
66% | With sodium amide In tetrahydrofuran | Rectangular plates of compound 35 were found suitable for X-ray diffraction, and a study was conducted. To complete the synthesis of bexarotene, the Friedel-Crafts acylation of 35, by crude mono-methyl-terephthaloyl chloride (36), gave ketone (37) which was converted to alkene ester(38) by a Wittig reaction, and ester 38 was saponified by potassium hydroxide followed by acidification with aqueous hydrochloric acid to give bexarotene (39) (Scheme 2). |
[ 1214741-14-6 ]
(S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate