AR066748A1 - Un proceso para la preparacion de compuestos de aminodiol protegidos con oxazolina utiles como intemediarios para florfenicol - Google Patents

Un proceso para la preparacion de compuestos de aminodiol protegidos con oxazolina utiles como intemediarios para florfenicol

Info

Publication number
AR066748A1
AR066748A1 ARP080102241A ARP080102241A AR066748A1 AR 066748 A1 AR066748 A1 AR 066748A1 AR P080102241 A ARP080102241 A AR P080102241A AR P080102241 A ARP080102241 A AR P080102241A AR 066748 A1 AR066748 A1 AR 066748A1
Authority
AR
Argentina
Prior art keywords
compound
formula
oxazoline
alkyl
phenyl
Prior art date
Application number
ARP080102241A
Other languages
English (en)
Original Assignee
Schering Plough Ltd
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 Schering Plough Ltd filed Critical Schering Plough Ltd
Publication of AR066748A1 publication Critical patent/AR066748A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/10Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D263/14Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/16Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C07C233/17Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/18Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C315/00Preparation of sulfones; Preparation of sulfoxides
    • C07C315/04Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings 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
    • C07D263/18Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Reivindicacion 1: Un proceso para la preparacion de un compuesto de aminodiol protegido con oxazolina, de la Formula (1), o una de sus sales de adicion de ácido: donde: R2 es hidrogeno, metiltio, metilsulfoxi, metilsulfonilo, fluormetiltio, fluormetilsulfoxi, fluormetilsulfonilo, nitro, fluor, bromo, cloro, acetilo, bencilo, fenilo, fenilo sustituido con halo, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-8, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, aralquilo C1-6, aralquenilo C2-6, o grupo heterocíclico C2-6; y R4 es hidrogeno, alquilo C1-6, haloalquilo C1-6, dihaloalquilo C1-6, trihaloalquilo C1-6, CH2Cl, CHCl2, CCl3, CH2Br, CHBr2, CBr3, CH2F, CHF2, CF3, cicloalquilo C3-8, ciclohaloalquilo C3-8, ciclodihaloalquilo C3-8, ciclotrihaloalquilo C3-8, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, aralquilo C1-6, aralquenilo C2-6, heterociclico C2-6, bencilo, o fenilo alquilo donde el fenilo o fenilo alquilo puede estar sustituido con uno o dos halogenos, alquilo C1-6 o alcoxi C1-6; donde el proceso comprende las etapas de: a) la reaccion de un compuesto de la Formula (2) o una de sus sales de adicion de ácido: (2) donde: R2 es corno se define con anterioridad; y R3 es hidrogeno, alquilo C1-6, cicloalquilo C3-8, bencilo, fenilo o alquilfenilo C1-6; con la condicion de que si el compuesto de la Formula (2) y es la sal de adicion de ácido, entonces la sal de adicion de ácido es la sal de HCI, HNO3, H2SO4, H3PO4 o la sal de ácido acético; con un reactivo promotor de amida, en un solvente formador de amida, con un compuesto promotor de amida, para formar un compuesto de éster amida de la Formula (3): donde R2, R3 y R4 se definen conforme a lo descripto con anterioridad: b) la reaccion del compuesto de la Formula (3) con un reactivo promotor de oxazolina, en un solvente formador de oxazolina, en presencia de un compuesto promotor de oxazolina, para formar un compuesto de éster oxazolina de la Formula (4): donde R2, R3 y R4 se definen segun lo descripto con anterioridad, y se presenta una estereoquímica relativa invertida en el carbono bencílico asimétrico, en comparacion con aquella del compuesto de la Formula (3); c) la reaccion del compuesto de la Formula (4) con una base de inversion de centro quiral en un solvente de inversion de centro quiral, para formar un compuesto de la Formula (5): donde R2, R3 y R4 se definen segun lo descripto con anterioridad, y donde se presenta una estereoquímica relativa invertida en el carbono de alfa-carbonilo asimétrico, en comparacion con aquella del compuesto de la Formula (4); y d) la reaccion del compuesto de la Formula (5) con un agente reductor, en un solvente promotor de la reduccion, para formar un compuesto de la Formula (6): donde R2 y R4 se definen segun lo descripto con anterioridad.
ARP080102241A 2007-05-30 2008-05-28 Un proceso para la preparacion de compuestos de aminodiol protegidos con oxazolina utiles como intemediarios para florfenicol AR066748A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US94078607P 2007-05-30 2007-05-30

Publications (1)

Publication Number Publication Date
AR066748A1 true AR066748A1 (es) 2009-09-09

Family

ID=39705084

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080102241A AR066748A1 (es) 2007-05-30 2008-05-28 Un proceso para la preparacion de compuestos de aminodiol protegidos con oxazolina utiles como intemediarios para florfenicol

Country Status (16)

Country Link
US (1) US20080319200A1 (es)
EP (1) EP2155702A1 (es)
JP (1) JP2010529016A (es)
KR (1) KR20100022999A (es)
CN (1) CN101784534A (es)
AR (1) AR066748A1 (es)
AU (1) AU2008260595A1 (es)
BR (1) BRPI0812297A2 (es)
CA (1) CA2688432A1 (es)
CL (1) CL2008001562A1 (es)
MX (1) MX2009013016A (es)
PE (1) PE20090758A1 (es)
RU (1) RU2009148864A (es)
TW (1) TW200904783A (es)
WO (1) WO2008150406A1 (es)
ZA (1) ZA200908404B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20050386A1 (es) 2003-05-29 2005-06-23 Schering Plough Ltd Composiciones farmaceuticas de florfenicol
CA2672795A1 (en) * 2006-12-13 2008-06-26 Schering-Plough Ltd. Water-soluble prodrugs of chloramphenicol, thiamphenicol, and analogs thereof
JP2011529895A (ja) 2008-07-30 2011-12-15 インターベツト・インターナシヨナル・ベー・ベー フロルフェニコール中間体として有用なオキサゾリン保護アミノジオール化合物を調製する方法
KR20180051676A (ko) 2009-10-16 2018-05-16 멜린타 테라퓨틱스, 인크. 항미생물성 화합물 및 이의 제조 방법 및 사용 방법
MX339000B (es) 2009-10-16 2016-05-09 Melinta Therapeutics Inc Compuestos antimicrobianos y metodos para fabricar y utilizar los mismos.
AU2012251438A1 (en) 2011-05-02 2013-11-14 Pfizer Inc. Novel cephalosporins useful as antibacterial agents
CN103254103A (zh) * 2013-06-05 2013-08-21 南通金利油脂工业有限公司 氟化剂在制备氟苯尼考工艺中的应用
CA2923214A1 (en) 2013-09-09 2015-03-12 Melinta Therapeutics, Inc. Antimicrobial compounds and methods of making and using the same
CA2923179A1 (en) 2013-09-09 2015-03-12 Melinta Therapeutics, Inc. Antimicrobial compounds and methods of making and using the same
CN103980166B (zh) * 2014-04-17 2016-06-22 天津大学 一种氟苯尼考的新晶型及其制备方法
EP3268370A4 (en) 2015-03-11 2018-08-22 Melinta Therapeutics, Inc. Antimicrobial compounds and methods of making and using the same
CN105218474B (zh) * 2015-10-22 2017-12-05 山东国邦药业股份有限公司 (4r,5r)‑2‑二氯甲基‑4,5‑二氢‑5‑(4‑甲砜基苯基)‑4‑恶唑甲醇的合成方法
CN106187837B (zh) * 2016-07-05 2020-03-20 和鼎(南京)医药技术有限公司 一种氟苯尼考中间体、及其制备方法和氟苯尼考的制备方法
CN106631872A (zh) * 2016-12-13 2017-05-10 浙江普洛家园药业有限公司 一种氟苯尼考类似物中间体的合成方法
CN109678811B (zh) * 2019-01-25 2020-12-29 湖北中牧安达药业有限公司 一种氟苯尼考中间体环合物的不对称制备方法
CN110330463B (zh) * 2019-08-02 2021-05-14 山东国邦药业有限公司 一种氟苯尼考中间体的制备方法
CN111285789A (zh) * 2020-03-16 2020-06-16 和鼎(南京)医药技术有限公司 制备氟苯尼考中间体的方法及由该方法得到的化合物
CN111423391A (zh) * 2020-03-18 2020-07-17 浙江康牧药业有限公司 一种氟苯尼考中间体的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE957484C (de) * 1950-03-24 1957-02-07 Parke Davis & Co Verfahren zur Herstellung von neuen Oxazolinabkoemmlingen
DE830956C (de) * 1950-05-23 1952-02-07 Parke Davis & Co Verfahren zur Herstellung von Aminodiolen
US2768972A (en) * 1951-03-13 1956-10-30 Centre Nat Rech Scient Preparation of n-acyl-beta aryl-serinols
US2816915A (en) * 1953-11-20 1957-12-17 Du Pont Separation of phenyl-serines
US5663361A (en) * 1996-08-19 1997-09-02 Schering Corporation Process for preparing intermediates to florfenicol
CN1173933C (zh) * 2001-06-01 2004-11-03 中国科学院上海有机化学研究所 一种从l型取代苯丝氨酸酯制备d-(-)-苏式1-r-取代苯基-2-二氯乙酰氨基-3-氟-1-丙醇的方法
CN1155553C (zh) * 2001-12-07 2004-06-30 中国科学院上海有机化学研究所 2-氟-α-甲基-[1,1’-二苯基]-4-乙酸的对映体的制备方法
TW200406372A (en) * 2002-03-08 2004-05-01 Schering Plough Ltd Novel florfenicol-type antibiotics

Also Published As

Publication number Publication date
BRPI0812297A2 (pt) 2014-11-25
CA2688432A1 (en) 2008-12-11
AU2008260595A1 (en) 2008-12-11
EP2155702A1 (en) 2010-02-24
MX2009013016A (es) 2010-02-17
ZA200908404B (en) 2010-08-25
AU2008260595A2 (en) 2010-01-07
PE20090758A1 (es) 2009-06-24
KR20100022999A (ko) 2010-03-03
TW200904783A (en) 2009-02-01
CL2008001562A1 (es) 2008-12-05
WO2008150406A1 (en) 2008-12-11
JP2010529016A (ja) 2010-08-26
RU2009148864A (ru) 2011-07-10
US20080319200A1 (en) 2008-12-25
CN101784534A (zh) 2010-07-21

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