CU20150165A7 - Proceso para la preparación de (2r,3r)-3-{[ 2-}[4-(s-ciclopropilsulfonimidoil)fenil]amino{ -5-(trifluorometil)pirimidin-4-il]oxi}butan-2-ol - Google Patents
Proceso para la preparación de (2r,3r)-3-{[ 2-}[4-(s-ciclopropilsulfonimidoil)fenil]amino{ -5-(trifluorometil)pirimidin-4-il]oxi}butan-2-olInfo
- Publication number
- CU20150165A7 CU20150165A7 CUP2015000165A CU20150165A CU20150165A7 CU 20150165 A7 CU20150165 A7 CU 20150165A7 CU P2015000165 A CUP2015000165 A CU P2015000165A CU 20150165 A CU20150165 A CU 20150165A CU 20150165 A7 CU20150165 A7 CU 20150165A7
- Authority
- CU
- Cuba
- Prior art keywords
- preparation
- cyclopropilsulfonimidoil
- trifluorometil
- pirimidin
- oxi
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/29—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/10—Compounds containing sulfur atoms doubly-bound to nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Abstract
La invención provee un nuevo proceso para la preparación deinhibidores de pan-CDK de la fórmula (I) ESPACIO PARA LA FÓRMULA que comprende pasos de alquilación, aminación oxidativa, oxidación, desprotección, separación de racemato, hidrogenación, preparación en dos etapas, acoplamiento, preparación de sales doblemente protegidas y separación de grupos protectores por hidrogenación y también por tratamiento con carbonato de potasio en metanol.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102010046720A DE102010046720A1 (de) | 2010-09-23 | 2010-09-23 | Verfahren zur Herstellung von pan-CDK-Inhibitoren der Formel (l), sowie Intermediate der Herstellung |
PCT/EP2011/066295 WO2012038411A1 (de) | 2010-09-23 | 2011-09-20 | Verfahren zur herstellung von pan-cdk-inhibitoren der formel (i), sowie intermediate der herstellung |
Publications (1)
Publication Number | Publication Date |
---|---|
CU20150165A7 true CU20150165A7 (es) | 2016-05-30 |
Family
ID=44677881
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CU2013000044A CU20130044A7 (es) | 2010-09-23 | 2013-03-22 | Proceso para la preparación de inhibidores de pan-cdk de fórmula (i), e intermediarios de la preparación |
CUP2015000165A CU20150165A7 (es) | 2010-09-23 | 2015-11-30 | Proceso para la preparación de (2r,3r)-3-{[ 2-}[4-(s-ciclopropilsulfonimidoil)fenil]amino{ -5-(trifluorometil)pirimidin-4-il]oxi}butan-2-ol |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CU2013000044A CU20130044A7 (es) | 2010-09-23 | 2013-03-22 | Proceso para la preparación de inhibidores de pan-cdk de fórmula (i), e intermediarios de la preparación |
Country Status (32)
Country | Link |
---|---|
US (1) | US9359306B2 (es) |
EP (1) | EP2619186A1 (es) |
JP (1) | JP5969993B2 (es) |
KR (1) | KR20130109145A (es) |
CN (1) | CN103119026B (es) |
AP (1) | AP2013006816A0 (es) |
AR (1) | AR083171A1 (es) |
AU (1) | AU2011304365B2 (es) |
BR (1) | BR112013006720A2 (es) |
CA (1) | CA2811807A1 (es) |
CL (1) | CL2013000797A1 (es) |
CO (1) | CO6690779A2 (es) |
CR (1) | CR20130138A (es) |
CU (2) | CU20130044A7 (es) |
DE (1) | DE102010046720A1 (es) |
DO (1) | DOP2013000063A (es) |
EC (1) | ECSP13012520A (es) |
GT (1) | GT201300078A (es) |
HK (1) | HK1185615A1 (es) |
IL (1) | IL225352A0 (es) |
MX (1) | MX2013003338A (es) |
MY (1) | MY160625A (es) |
NZ (1) | NZ608448A (es) |
PE (1) | PE20140182A1 (es) |
RU (1) | RU2585621C2 (es) |
SA (1) | SA111320775B1 (es) |
SG (1) | SG188967A1 (es) |
TW (1) | TWI530488B (es) |
UA (1) | UA110626C2 (es) |
UY (1) | UY33624A (es) |
WO (1) | WO2012038411A1 (es) |
ZA (1) | ZA201301799B (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201418243A (zh) | 2012-11-15 | 2014-05-16 | Bayer Pharma AG | 含有磺醯亞胺基團之n-(吡啶-2-基)嘧啶-4-胺衍生物 |
WO2014173815A1 (en) * | 2013-04-23 | 2014-10-30 | Bayer Pharma Aktiengesellschaft | Use of (rs)-s-cyclopropyl-s-(4-{[4-{[(1r, 2r)-2-hydroxy-1-methylpropyl]oxy}-5- (trifluoromethyl)pyrimidin-2-yl]amino}phenyl)sulphoximide for the treatment of specific tumours |
AR113344A1 (es) | 2017-10-05 | 2020-04-22 | Innovative Molecules Gmbh | Enantiómeros de una serie de compuestos antivirales |
AU2019221019B2 (en) | 2018-02-13 | 2024-05-02 | Bayer Ag | Use of 5-Fluoro-4-(4-fluoro-2-methoxyphenyl)-N-{4-[(S-methylsulfonimidoyl)methyl]pyridin-2-yl}pyridin-2-amine for treating diffuse large B-cell lymphoma |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA964426B (en) * | 1995-06-05 | 1997-03-06 | Rhone Poulenc Agrochimie | Pesticidal sulfur compounds |
EP1291336A3 (en) | 2001-09-05 | 2003-10-08 | Solvias AG | Preparation of optically active alpha-hydroxyethers |
DE10349423A1 (de) * | 2003-10-16 | 2005-06-16 | Schering Ag | Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
DE102005062742A1 (de) * | 2005-12-22 | 2007-06-28 | Bayer Schering Pharma Ag | Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel |
EP2022785A1 (en) * | 2007-06-20 | 2009-02-11 | Bayer Schering Pharma Aktiengesellschaft | Alkynylpyrimidines as Tie2 kinase inhibitors |
EP2179991A1 (de) | 2008-10-21 | 2010-04-28 | Bayer Schering Pharma Aktiengesellschaft | Sulfoximinsubstituierte Anilino-Pyrimidinderivate als CDK-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
-
2010
- 2010-09-23 DE DE102010046720A patent/DE102010046720A1/de not_active Withdrawn
-
2011
- 2011-09-20 BR BR112013006720A patent/BR112013006720A2/pt not_active IP Right Cessation
- 2011-09-20 AU AU2011304365A patent/AU2011304365B2/en not_active Ceased
- 2011-09-20 WO PCT/EP2011/066295 patent/WO2012038411A1/de active Application Filing
- 2011-09-20 RU RU2013118432/04A patent/RU2585621C2/ru not_active IP Right Cessation
- 2011-09-20 UA UAA201305209A patent/UA110626C2/uk unknown
- 2011-09-20 JP JP2013529628A patent/JP5969993B2/ja not_active Expired - Fee Related
- 2011-09-20 MX MX2013003338A patent/MX2013003338A/es not_active Application Discontinuation
- 2011-09-20 SG SG2013018361A patent/SG188967A1/en unknown
- 2011-09-20 KR KR1020137010236A patent/KR20130109145A/ko not_active Application Discontinuation
- 2011-09-20 CA CA2811807A patent/CA2811807A1/en not_active Abandoned
- 2011-09-20 MY MYPI2013000997A patent/MY160625A/en unknown
- 2011-09-20 US US13/824,160 patent/US9359306B2/en not_active Expired - Fee Related
- 2011-09-20 CN CN201180045115.7A patent/CN103119026B/zh not_active Expired - Fee Related
- 2011-09-20 EP EP11761054.3A patent/EP2619186A1/de not_active Withdrawn
- 2011-09-20 NZ NZ608448A patent/NZ608448A/en not_active IP Right Cessation
- 2011-09-20 AP AP2013006816A patent/AP2013006816A0/xx unknown
- 2011-09-20 PE PE2013000617A patent/PE20140182A1/es not_active Application Discontinuation
- 2011-09-21 SA SA111320775A patent/SA111320775B1/ar unknown
- 2011-09-22 UY UY0001033624A patent/UY33624A/es unknown
- 2011-09-23 TW TW100134438A patent/TWI530488B/zh active
- 2011-09-23 AR ARP110103498A patent/AR083171A1/es not_active Application Discontinuation
-
2013
- 2013-03-08 ZA ZA2013/01799A patent/ZA201301799B/en unknown
- 2013-03-20 IL IL225352A patent/IL225352A0/en unknown
- 2013-03-22 DO DO2013000063A patent/DOP2013000063A/es unknown
- 2013-03-22 CR CR20130138A patent/CR20130138A/es unknown
- 2013-03-22 CU CU2013000044A patent/CU20130044A7/es unknown
- 2013-03-22 EC ECSP13012520 patent/ECSP13012520A/es unknown
- 2013-03-22 CO CO13057092A patent/CO6690779A2/es unknown
- 2013-03-22 CL CL2013000797A patent/CL2013000797A1/es unknown
- 2013-03-22 GT GT201300078A patent/GT201300078A/es unknown
- 2013-11-21 HK HK13113029.3A patent/HK1185615A1/xx not_active IP Right Cessation
-
2015
- 2015-11-30 CU CUP2015000165A patent/CU20150165A7/es unknown
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