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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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&gt;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). 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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&gt;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). 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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&gt;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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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title Processo para a preparação de derivados de 2,2-difluoroetilamina através da hidrogenação de imina
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