ΜΕΘΟΔΟΣ ΠΑΡΑΓΩΓΗΣ ΕΝΟΣ ΠΑΡΑΓΩΓΟΥ ΒΕΝΖΙΜΙΔΑΖΟΛΙΟΥ

Η εφεύρεση σχετίζεται με μια μέθοδο παρασκευής της ένωσης του τύπου 1, ενός πολυτίμου ενδιάμεσου προϊόντος στη σύνθεση της φαρμακευτικής δραστικής ουσίας ετεξιλική δαβιγατράνη. Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-prop...

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Hauptverfasser: SOBOTTA RAINER, BROEDER WOLFGANG
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BROEDER WOLFGANG
description Η εφεύρεση σχετίζεται με μια μέθοδο παρασκευής της ένωσης του τύπου 1, ενός πολυτίμου ενδιάμεσου προϊόντος στη σύνθεση της φαρμακευτικής δραστικής ουσίας ετεξιλική δαβιγατράνη. Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (I) involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of (IV) (V), which is converted to (I). Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (I) optionally in the form of its acid addition salt involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (V), which is converted to (I). An independent claim is included for new intermediate hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (V). [Image].
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fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CY1111045TT1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CY1111045TT1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CY1111045TT13</originalsourceid><addsrcrecordid>eNrjZIg5N-fc1HMzzs0_NwWIFyucW3Bu4rmFQDz53Eogng4SmnpuLja5-eeWKpybBJaddm4m0JyZQDMmAtnzz80GsoHSPAysaYk5xam8UJqbQdHNNcTZQze1ID8-tbggMTk1L7Uk3jnSEAgMTExDQgyNiVEDAFkBWBk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>ΜΕΘΟΔΟΣ ΠΑΡΑΓΩΓΗΣ ΕΝΟΣ ΠΑΡΑΓΩΓΟΥ ΒΕΝΖΙΜΙΔΑΖΟΛΙΟΥ</title><source>esp@cenet</source><creator>SOBOTTA RAINER ; BROEDER WOLFGANG</creator><creatorcontrib>SOBOTTA RAINER ; BROEDER WOLFGANG</creatorcontrib><description>Η εφεύρεση σχετίζεται με μια μέθοδο παρασκευής της ένωσης του τύπου 1, ενός πολυτίμου ενδιάμεσου προϊόντος στη σύνθεση της φαρμακευτικής δραστικής ουσίας ετεξιλική δαβιγατράνη. Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (I) involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of (IV) (V), which is converted to (I). Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (I) optionally in the form of its acid addition salt involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (V), which is converted to (I). An independent claim is included for new intermediate hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (V). [Image].</description><language>Greek</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&amp;date=20150611&amp;DB=EPODOC&amp;CC=CY&amp;NR=1111045T1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20150611&amp;DB=EPODOC&amp;CC=CY&amp;NR=1111045T1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SOBOTTA RAINER</creatorcontrib><creatorcontrib>BROEDER WOLFGANG</creatorcontrib><title>ΜΕΘΟΔΟΣ ΠΑΡΑΓΩΓΗΣ ΕΝΟΣ ΠΑΡΑΓΩΓΟΥ ΒΕΝΖΙΜΙΔΑΖΟΛΙΟΥ</title><description>Η εφεύρεση σχετίζεται με μια μέθοδο παρασκευής της ένωσης του τύπου 1, ενός πολυτίμου ενδιάμεσου προϊόντος στη σύνθεση της φαρμακευτικής δραστικής ουσίας ετεξιλική δαβιγατράνη. Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (I) involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of (IV) (V), which is converted to (I). Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (I) optionally in the form of its acid addition salt involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (V), which is converted to (I). An independent claim is included for new intermediate hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (V). 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Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (I) involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of (IV) (V), which is converted to (I). Preparation of 3-({2-[(4-carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (I) optionally in the form of its acid addition salt involves reacting 3-[(3-amino-4-methylamino-benzoyl)-pyridin-2-yl-amino]-propionic acid ethyl ester (II) with (4-cyano-phenylamino)-acetic acid (III) in presence of coupling agent to form 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (IV), which is converted without isolation into hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester of formula (V), which is converted to (I). An independent claim is included for new intermediate hydrobromide salt of 3-({2-[(4-cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-pyridin-2-yl-amino)-propionic acid ethyl ester (V). [Image].</abstract><oa>free_for_read</oa></addata></record>
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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title ΜΕΘΟΔΟΣ ΠΑΡΑΓΩΓΗΣ ΕΝΟΣ ΠΑΡΑΓΩΓΟΥ ΒΕΝΖΙΜΙΔΑΖΟΛΙΟΥ
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