Process for the preparation of chemical compounds
The invention provides a process for preparing a compound of formula (I)and pharmaceutically acceptable derivatives thereof wherein:R and R are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms;R is H, C1-6alkyl, C1-6alkyl substitu...
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creator | FITZGERALD RUSS N JUNG DAVID KENDALL EADDY JOHN F |
description | The invention provides a process for preparing a compound of formula (I)and pharmaceutically acceptable derivatives thereof wherein:R and R are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms;R is H, C1-6alkyl, C1-6alkyl substituted by one or more fluorine atoms, C1-6alkoxy, C1-6hydroxyalkyl, SC1-6alkyl, C(O)H, C(O)C1-6alkyl, C1-6alkylsulfonyl, C1-6alkoxy substituted by one or more fluorine atoms, halogen, CN, CONR R , CO2H, CO2C1-6alkyl, or NHSO2R ;R is H or phenyl substituted by SO2C1-6alkyl or SO2NH2;R and R are independently selected from H, C1-6alkyl, phenyl, phenyl substituted by one or more atoms or groups R , or together with the nitrogen atom to which they are attached form a saturated 4 to 8 membered ringR is halogen, C1-6alkyl, C1-6alkoxy or C1-6alkoxy substituted by one or more fluorine atoms;which comprises rearrangement of an azirine of formula (II)wherein R to R are as defined for formula (I), or a protected derivative thereof, in the presence of a catalyst and a solvent. |
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HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2004</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20040629&DB=EPODOC&CC=US&NR=6756498B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20040629&DB=EPODOC&CC=US&NR=6756498B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>FITZGERALD RUSS N</creatorcontrib><creatorcontrib>JUNG DAVID KENDALL</creatorcontrib><creatorcontrib>EADDY JOHN F</creatorcontrib><title>Process for the preparation of chemical compounds</title><description>The invention provides a process for preparing a compound of formula (I)and pharmaceutically acceptable derivatives thereof wherein:R and R are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms;R is H, C1-6alkyl, C1-6alkyl substituted by one or more fluorine atoms, C1-6alkoxy, C1-6hydroxyalkyl, SC1-6alkyl, C(O)H, C(O)C1-6alkyl, C1-6alkylsulfonyl, C1-6alkoxy substituted by one or more fluorine atoms, halogen, CN, CONR R , CO2H, CO2C1-6alkyl, or NHSO2R ;R is H or phenyl substituted by SO2C1-6alkyl or SO2NH2;R and R are independently selected from H, C1-6alkyl, phenyl, phenyl substituted by one or more atoms or groups R , or together with the nitrogen atom to which they are attached form a saturated 4 to 8 membered ringR is halogen, C1-6alkyl, C1-6alkoxy or C1-6alkoxy substituted by one or more fluorine atoms;which comprises rearrangement of an azirine of formula (II)wherein R to R are as defined for formula (I), or a protected derivative thereof, in the presence of a catalyst and a solvent.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2004</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDAMKMpPTi0uVkjLL1IoyUhVKChKLUgsSizJzM9TyE9TSM5Izc1MTsxRSM7PLcgvzUsp5mFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8aHBZuamZiaWFk5GxkQoAQBReyuz</recordid><startdate>20040629</startdate><enddate>20040629</enddate><creator>FITZGERALD RUSS N</creator><creator>JUNG DAVID KENDALL</creator><creator>EADDY JOHN F</creator><scope>EVB</scope></search><sort><creationdate>20040629</creationdate><title>Process for the preparation of chemical compounds</title><author>FITZGERALD RUSS N ; JUNG DAVID KENDALL ; EADDY JOHN F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US6756498B23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2004</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>FITZGERALD RUSS N</creatorcontrib><creatorcontrib>JUNG DAVID KENDALL</creatorcontrib><creatorcontrib>EADDY JOHN F</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>FITZGERALD RUSS N</au><au>JUNG DAVID KENDALL</au><au>EADDY JOHN F</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for the preparation of chemical compounds</title><date>2004-06-29</date><risdate>2004</risdate><abstract>The invention provides a process for preparing a compound of formula (I)and pharmaceutically acceptable derivatives thereof wherein:R and R are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms;R is H, C1-6alkyl, C1-6alkyl substituted by one or more fluorine atoms, C1-6alkoxy, C1-6hydroxyalkyl, SC1-6alkyl, C(O)H, C(O)C1-6alkyl, C1-6alkylsulfonyl, C1-6alkoxy substituted by one or more fluorine atoms, halogen, CN, CONR R , CO2H, CO2C1-6alkyl, or NHSO2R ;R is H or phenyl substituted by SO2C1-6alkyl or SO2NH2;R and R are independently selected from H, C1-6alkyl, phenyl, phenyl substituted by one or more atoms or groups R , or together with the nitrogen atom to which they are attached form a saturated 4 to 8 membered ringR is halogen, C1-6alkyl, C1-6alkoxy or C1-6alkoxy substituted by one or more fluorine atoms;which comprises rearrangement of an azirine of formula (II)wherein R to R are as defined for formula (I), or a protected derivative thereof, in the presence of a catalyst and a solvent.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Process for the preparation of chemical compounds |
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