Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina
Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative (IV) to the corresponding 2,2-difluoroethylamine-derivative (III). Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C...
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creator | NORBERT LUI JENS-DIETMAR HEINRICH |
description | Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative (IV) to the corresponding 2,2-difluoroethylamine-derivative (III). Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C(F) 2) (IV) to the corresponding 2,2-difluoroethylamine-derivative of formula (A-CH 2-NH-CH 2-C(F) 2) (III). A : pyrid-2-yl, pyrid-4-yl or pyrid-3-yl (all optionally substituted by F, Cl, Br, CH 3, CF 3or CF 3O (at 6th position)) or pyridazin-3-yl (optionally substituted by Cl or CH 3(at 6th position)), and pyrazin-3-yl, 2-chloropyrazin-5-yl or 1,3-thiazol-5-yl (all optionally substituted by Cl or CH 3(at 2nd position)), or pyrimidinyl, pyrazolyl, thiophenyl, oxazolyl, isoxazolyl, 1,2,4-oxadiazolyl, isothiazolyl, 1,2,4-triazolyl or 1,2,5-thiadiazolyl (all optionally substituted by F, Cl, Br, CN, NO 2, 1-4C-alkyl (optionally substituted by F and/or Cl), 1-3C-alkylthio (optionally substituted by F and/or Cl), 1-3C-alkylsulfonyl (optionally substituted by F and/or Cl)) or substituted pyridine moiety of formula (A1); X : halo, alkyl or haloalkyl; and Y 1>halo, alkyl, haloalkyl, haloalkoxy, azido or cyano-group. Independent claims are included for: (1) preparing 2,2-difluoroethylimine-derivative of formula (IV) comprising reacting a carbonyl compound of formula (A-C(=O)-H) (VI) with 2,2-difluoroethylamine; and (2) the 2,2-difluoroethylimine-derivative (IV). [Image]. |
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Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C(F) 2) (IV) to the corresponding 2,2-difluoroethylamine-derivative of formula (A-CH 2-NH-CH 2-C(F) 2) (III). A : pyrid-2-yl, pyrid-4-yl or pyrid-3-yl (all optionally substituted by F, Cl, Br, CH 3, CF 3or CF 3O (at 6th position)) or pyridazin-3-yl (optionally substituted by Cl or CH 3(at 6th position)), and pyrazin-3-yl, 2-chloropyrazin-5-yl or 1,3-thiazol-5-yl (all optionally substituted by Cl or CH 3(at 2nd position)), or pyrimidinyl, pyrazolyl, thiophenyl, oxazolyl, isoxazolyl, 1,2,4-oxadiazolyl, isothiazolyl, 1,2,4-triazolyl or 1,2,5-thiadiazolyl (all optionally substituted by F, Cl, Br, CN, NO 2, 1-4C-alkyl (optionally substituted by F and/or Cl), 1-3C-alkylthio (optionally substituted by F and/or Cl), 1-3C-alkylsulfonyl (optionally substituted by F and/or Cl)) or substituted pyridine moiety of formula (A1); X : halo, alkyl or haloalkyl; and Y 1>halo, alkyl, haloalkyl, haloalkoxy, azido or cyano-group. Independent claims are included for: (1) preparing 2,2-difluoroethylimine-derivative of formula (IV) comprising reacting a carbonyl compound of formula (A-C(=O)-H) (VI) with 2,2-difluoroethylamine; and (2) the 2,2-difluoroethylimine-derivative (IV). [Image].</description><language>por</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2015</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=20150317&DB=EPODOC&CC=BR&NR=PI0816868A2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,309,781,886,25568,76551</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20150317&DB=EPODOC&CC=BR&NR=PI0816868A2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NORBERT LUI</creatorcontrib><creatorcontrib>JENS-DIETMAR HEINRICH</creatorcontrib><title>Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina</title><description>Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative (IV) to the corresponding 2,2-difluoroethylamine-derivative (III). Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C(F) 2) (IV) to the corresponding 2,2-difluoroethylamine-derivative of formula (A-CH 2-NH-CH 2-C(F) 2) (III). A : pyrid-2-yl, pyrid-4-yl or pyrid-3-yl (all optionally substituted by F, Cl, Br, CH 3, CF 3or CF 3O (at 6th position)) or pyridazin-3-yl (optionally substituted by Cl or CH 3(at 6th position)), and pyrazin-3-yl, 2-chloropyrazin-5-yl or 1,3-thiazol-5-yl (all optionally substituted by Cl or CH 3(at 2nd position)), or pyrimidinyl, pyrazolyl, thiophenyl, oxazolyl, isoxazolyl, 1,2,4-oxadiazolyl, isothiazolyl, 1,2,4-triazolyl or 1,2,5-thiadiazolyl (all optionally substituted by F, Cl, Br, CN, NO 2, 1-4C-alkyl (optionally substituted by F and/or Cl), 1-3C-alkylthio (optionally substituted by F and/or Cl), 1-3C-alkylsulfonyl (optionally substituted by F and/or Cl)) or substituted pyridine moiety of formula (A1); X : halo, alkyl or haloalkyl; and Y 1>halo, alkyl, haloalkyl, haloalkoxy, azido or cyano-group. Independent claims are included for: (1) preparing 2,2-difluoroethylimine-derivative of formula (IV) comprising reacting a carbonyl compound of formula (A-C(=O)-H) (VI) with 2,2-difluoroethylamine; and (2) the 2,2-difluoroethylimine-derivative (IV). [Image].</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2015</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZEgLKMpPTi0uzlcoSCxKVEhUKChKBbEOLz-8OF8hJRWIijLLElPyi0EcIx0j3ZTMtJzS_KL81JLMnMTczDygppKixLLDK4EqEhUyMlOK8tNT8xAGZILU8DCwpiXmFKfyQmluBiU31xBnD93Ugvz41OKCxOTUvNSSeKegAE8DC0MzCzMLRyNjohQBAC78QuM</recordid><startdate>20150317</startdate><enddate>20150317</enddate><creator>NORBERT LUI</creator><creator>JENS-DIETMAR HEINRICH</creator><scope>EVB</scope></search><sort><creationdate>20150317</creationdate><title>Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina</title><author>NORBERT LUI ; JENS-DIETMAR HEINRICH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_BRPI0816868A23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>por</language><creationdate>2015</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>NORBERT LUI</creatorcontrib><creatorcontrib>JENS-DIETMAR HEINRICH</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NORBERT LUI</au><au>JENS-DIETMAR HEINRICH</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina</title><date>2015-03-17</date><risdate>2015</risdate><abstract>Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative (IV) to the corresponding 2,2-difluoroethylamine-derivative (III). Preparing 2,2-difluoroethylamine-derivatives comprises hydrogenating 2,2-difluoroethylimine-derivative of formula (A-CH 2=N-CH 2-C(F) 2) (IV) to the corresponding 2,2-difluoroethylamine-derivative of formula (A-CH 2-NH-CH 2-C(F) 2) (III). A : pyrid-2-yl, pyrid-4-yl or pyrid-3-yl (all optionally substituted by F, Cl, Br, CH 3, CF 3or CF 3O (at 6th position)) or pyridazin-3-yl (optionally substituted by Cl or CH 3(at 6th position)), and pyrazin-3-yl, 2-chloropyrazin-5-yl or 1,3-thiazol-5-yl (all optionally substituted by Cl or CH 3(at 2nd position)), or pyrimidinyl, pyrazolyl, thiophenyl, oxazolyl, isoxazolyl, 1,2,4-oxadiazolyl, isothiazolyl, 1,2,4-triazolyl or 1,2,5-thiadiazolyl (all optionally substituted by F, Cl, Br, CN, NO 2, 1-4C-alkyl (optionally substituted by F and/or Cl), 1-3C-alkylthio (optionally substituted by F and/or Cl), 1-3C-alkylsulfonyl (optionally substituted by F and/or Cl)) or substituted pyridine moiety of formula (A1); X : halo, alkyl or haloalkyl; and Y 1>halo, alkyl, haloalkyl, haloalkoxy, azido or cyano-group. Independent claims are included for: (1) preparing 2,2-difluoroethylimine-derivative of formula (IV) comprising reacting a carbonyl compound of formula (A-C(=O)-H) (VI) with 2,2-difluoroethylamine; and (2) the 2,2-difluoroethylimine-derivative (IV). [Image].</abstract><oa>free_for_read</oa></addata></record> |
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title | Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina |
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