SMT201300116B - Procedimenti e intermedi per la preparazione di uninibitore macrociclico di proteasi di hcv - Google Patents

Procedimenti e intermedi per la preparazione di uninibitore macrociclico di proteasi di hcv

Info

Publication number
SMT201300116B
SMT201300116B SM201300116T SM201300116T SMT201300116B SM T201300116 B SMT201300116 B SM T201300116B SM 201300116 T SM201300116 T SM 201300116T SM 201300116 T SM201300116 T SM 201300116T SM T201300116 B SMT201300116 B SM T201300116B
Authority
SM
San Marino
Prior art keywords
intermediates
preparation
hcv
procedures
protease inhibitor
Prior art date
Application number
SM201300116T
Other languages
English (en)
Italian (it)
Inventor
Andras Horvath
Dominic John Ormerod
Dominique Paul Michel Depre
Veronique Cerpentier
Original Assignee
Janssen Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Janssen Pharmaceuticals Inc filed Critical Janssen Pharmaceuticals Inc
Publication of SMT201300116B publication Critical patent/SMT201300116B/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/40Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/475Preparation of carboxylic acid esters by splitting of carbon-to-carbon bonds and redistribution, e.g. disproportionation or migration of groups between different molecules
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/32Oxygen atoms
    • C07D307/33Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • C07D453/04Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Furan Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
SM201300116T 2008-12-23 2013-10-10 Procedimenti e intermedi per la preparazione di uninibitore macrociclico di proteasi di hcv SMT201300116B (it)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08172691 2008-12-23
PCT/EP2009/067715 WO2010072742A1 (en) 2008-12-23 2009-12-22 Processes and intermediates for preparing a macrocyclic protease inhibitor of hcv

Publications (1)

Publication Number Publication Date
SMT201300116B true SMT201300116B (it) 2013-11-08

Family

ID=40548041

Family Applications (1)

Application Number Title Priority Date Filing Date
SM201300116T SMT201300116B (it) 2008-12-23 2013-10-10 Procedimenti e intermedi per la preparazione di uninibitore macrociclico di proteasi di hcv

Country Status (22)

Country Link
US (2) US8927722B2 (https=)
EP (1) EP2382198B1 (https=)
JP (1) JP5687631B2 (https=)
KR (1) KR101734507B1 (https=)
CN (1) CN102264715B (https=)
AR (1) AR074863A1 (https=)
AU (1) AU2009331530B2 (https=)
BR (1) BRPI0923393B1 (https=)
CA (1) CA2745565C (https=)
CY (1) CY1114488T1 (https=)
DK (1) DK2382198T3 (https=)
ES (1) ES2429013T3 (https=)
HR (1) HRP20130906T1 (https=)
IL (1) IL213246A (https=)
MX (1) MX2011006764A (https=)
PL (1) PL2382198T3 (https=)
PT (1) PT2382198E (https=)
RU (1) RU2016120007A (https=)
SI (1) SI2382198T1 (https=)
SM (1) SMT201300116B (https=)
TW (1) TWI461424B (https=)
WO (1) WO2010072742A1 (https=)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5687631B2 (ja) 2008-12-23 2015-03-18 ジヤンセン・フアーマシユーチカルズ・インコーポレーテツドJanssen Pharmaceuticals,Inc. Hcvのマクロ環状プロテアーゼ阻害剤を製造するための方法および中間体
CA2845720A1 (en) 2011-09-22 2013-03-28 Janssen Pharmaceuticals, Inc. Processes and intermediates for preparing a macrocyclic protease inhibitor of hcv
TWI574960B (zh) * 2011-10-28 2017-03-21 健生醫藥公司 用於製備大環蛋白酶抑制劑tmc435之中間體的改良方法
CN103387509B (zh) * 2012-05-11 2016-06-08 重庆博腾制药科技股份有限公司 一种hcv蛋白酶抑制剂中间体的制备方法
EA026235B1 (ru) * 2012-06-08 2017-03-31 Джилид Сайэнс, Инк. Макроциклические ингибиторы вирусов flaviviridae
PT2859009T (pt) 2012-06-08 2018-01-18 Gilead Sciences Inc Inibidores macrocíclicos dos vírus flaviviridae
AR091279A1 (es) 2012-06-08 2015-01-21 Gilead Sciences Inc Inhibidores macrociclicos de virus flaviviridae
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
US9617310B2 (en) 2013-03-15 2017-04-11 Gilead Sciences, Inc. Inhibitors of hepatitis C virus
CN105308043B (zh) * 2014-05-29 2018-01-30 杭州普晒医药科技有限公司 丙型肝炎药物的晶型及其制备方法、其药物组合物和用途
MA41812A (fr) 2015-03-27 2018-01-30 Janssen Pharmaceuticals Inc Procédés et intermédiaires pour la préparation d'un inhibiteur de protéase macrocyclique du vhc

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL8300536A (nl) 1983-02-14 1984-09-03 Oce Andeno Bv Optisch actief alfa-azido-p-hydroxyfenylazijnzuur en zijn zouten alsmede de bereiding daarvan.
JPS6124539A (ja) 1984-07-11 1986-02-03 Sagami Chem Res Center 光学活性(r)−2,5,12−トリヒドロキシ−1,2,3,4−テトラヒドロナフタセン−6,11−ジオン−2−カルボン酸の取得方法
JP4218040B2 (ja) 1997-12-26 2009-02-04 曽田香料株式会社 有機酸とアミンの複合塩の製造法
JP3844112B2 (ja) 2000-08-23 2006-11-08 高砂香料工業株式会社 3,5,6−トリヒドロキシヘキサン酸アンモニウム塩誘導体、及びその製造方法
PL1713822T3 (pl) 2004-01-30 2010-08-31 Medivir Ab Inhibitory proteazy serynowej HCV NS-3
CN101146794A (zh) * 2005-01-21 2008-03-19 阿斯泰克斯治疗有限公司 用于抑制cdk和gsk的吡唑衍生物
PE20070211A1 (es) 2005-07-29 2007-05-12 Medivir Ab Compuestos macrociclicos como inhibidores del virus de hepatitis c
US8012939B2 (en) * 2005-07-29 2011-09-06 Tibotec Pharmaceuticals Ltd. Co Macrocyclic inhibitors of hepatitis C virus
DE602008001251D1 (de) * 2007-02-01 2010-06-24 Tibotec Pharm Ltd Verfahren und zwischenprodukte zur herstellung eines makrozyklischen proteasehemmers von hcv
BRPI0807482A2 (pt) * 2007-02-08 2014-05-13 Tibotec Pharm Ltd Fenilcarbamatos macrocíclicos inibidores de hcv
JP5687631B2 (ja) 2008-12-23 2015-03-18 ジヤンセン・フアーマシユーチカルズ・インコーポレーテツドJanssen Pharmaceuticals,Inc. Hcvのマクロ環状プロテアーゼ阻害剤を製造するための方法および中間体

Also Published As

Publication number Publication date
BRPI0923393A2 (pt) 2015-07-28
JP5687631B2 (ja) 2015-03-18
TWI461424B (zh) 2014-11-21
AU2009331530B2 (en) 2015-04-09
AU2009331530A1 (en) 2011-06-23
CA2745565A1 (en) 2010-07-01
SI2382198T1 (sl) 2013-11-29
CA2745565C (en) 2017-03-07
KR20110099048A (ko) 2011-09-05
AR074863A1 (es) 2011-02-16
CN102264715A (zh) 2011-11-30
KR101734507B1 (ko) 2017-05-11
JP2012513381A (ja) 2012-06-14
US20150080577A1 (en) 2015-03-19
PL2382198T3 (pl) 2013-11-29
MX2011006764A (es) 2011-08-03
ES2429013T3 (es) 2013-11-12
EP2382198A1 (en) 2011-11-02
IL213246A (en) 2017-10-31
WO2010072742A1 (en) 2010-07-01
US8927722B2 (en) 2015-01-06
EP2382198B1 (en) 2013-07-10
BRPI0923393B1 (pt) 2018-06-19
CY1114488T1 (el) 2016-10-05
CN102264715B (zh) 2015-12-02
HRP20130906T1 (hr) 2013-10-25
PT2382198E (pt) 2013-10-01
HK1164839A1 (zh) 2012-09-28
RU2011130895A (ru) 2013-01-27
US9115077B2 (en) 2015-08-25
US20110257403A1 (en) 2011-10-20
DK2382198T3 (da) 2013-09-30
RU2016120007A (ru) 2018-11-13
IL213246A0 (en) 2011-07-31
TW201033205A (en) 2010-09-16

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