AR003509A1 - Sintesis de alfa-cloro o fluoro cetonas. - Google Patents

Sintesis de alfa-cloro o fluoro cetonas.

Info

Publication number
AR003509A1
AR003509A1 ARP960104240A AR10424096A AR003509A1 AR 003509 A1 AR003509 A1 AR 003509A1 AR P960104240 A ARP960104240 A AR P960104240A AR 10424096 A AR10424096 A AR 10424096A AR 003509 A1 AR003509 A1 AR 003509A1
Authority
AR
Argentina
Prior art keywords
formula
chlorine
compound
fluorine
phenyl
Prior art date
Application number
ARP960104240A
Other languages
English (en)
Original Assignee
Merck & Co 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
Priority claimed from GBGB9602925.1A external-priority patent/GB9602925D0/en
Application filed by Merck & Co Inc filed Critical Merck & Co Inc
Publication of AR003509A1 publication Critical patent/AR003509A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C319/00Preparation of thiols, sulfides, hydropolysulfides or polysulfides
    • C07C319/14Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
    • C07C319/20Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/004Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with organometalhalides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/54Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Una síntesis simple, de alto rendimiento, de alfa-cloro cetonas, de la fórmula (I) donde Y es cloro o flúor y A es un nucleófilo de carbono quecomprende: (a) hacer reaccionar un reactivo organometálico de fórmula (A-M) en donde M es Li o Mg, con un compuesto de fórmula (III), en donde X es -NR(OR1);R y R1 son cada uno, independientemente, alquil C1-3 lineal o ramificado, cicloalquil C3-6 u opcionalmente substituido con alcoxi C1-3, fenil, fenilsubstituido, en donde el substituto en el fenil se selecciona de F, Cl, Br, metiltio, -OH, metoxi, aminotio y alquil C1-3;en un solvente orgánico aprótico,y (b) hacer reaccionar sin purificación adicional al producto del paso (a) con una solución acuosa de ácido G, para dar una fase con solvente orgánicoaprótico que comprende un compuesto de fórmula (I) y una fase de solvente acuoso que comprende a un compuesto de fórmula (III). En la fórmula (I), Y escloro o fluor y A es un nucleófilo de carbono, que abarca la acilación dereactivos de Grignard y de organolitio con N-metoxi-N-metilcloracetamida. Laeficiencia del procedimiento se mejora ulteriormente reciclando la N,O- dimetilhidroxilamina.
ARP960104240A 1995-09-15 1996-09-05 Sintesis de alfa-cloro o fluoro cetonas. AR003509A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US382395P 1995-09-15 1995-09-15
GBGB9602925.1A GB9602925D0 (en) 1996-02-13 1996-02-13 Synthesis of a-chloro or fluoro ketones

Publications (1)

Publication Number Publication Date
AR003509A1 true AR003509A1 (es) 1998-08-05

Family

ID=26308680

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960104240A AR003509A1 (es) 1995-09-15 1996-09-05 Sintesis de alfa-cloro o fluoro cetonas.

Country Status (18)

Country Link
EP (1) EP0851850B1 (es)
CN (1) CN1101374C (es)
AR (1) AR003509A1 (es)
AT (1) ATE210624T1 (es)
AU (1) AU6973896A (es)
BR (1) BR9610272A (es)
CZ (1) CZ290202B6 (es)
DE (1) DE69617969T2 (es)
DK (1) DK0851850T3 (es)
EA (1) EA001935B1 (es)
ES (1) ES2167600T3 (es)
HK (1) HK1010189A1 (es)
PT (1) PT851850E (es)
RO (1) RO120706B1 (es)
SK (1) SK282779B6 (es)
TW (1) TW338032B (es)
UA (1) UA57001C2 (es)
WO (1) WO1997010195A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE280167T1 (de) 1999-07-23 2004-11-15 Pfizer Prod Inc Zwischenprodukte und ein verfahren zur herstellung von beta3-adrenergischer rezeptor- agoniste
CN107746388B (zh) * 2017-11-23 2021-01-01 江苏恒盛药业有限公司 一种伏立康唑中间体的制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1596278A (en) * 1976-11-30 1981-08-26 Glaxo Operations Ltd 7-(-oxyimino-acetamino)cephalosporin derivatives

Also Published As

Publication number Publication date
CN1101374C (zh) 2003-02-12
EP0851850A1 (en) 1998-07-08
WO1997010195A1 (en) 1997-03-20
CZ290202B6 (cs) 2002-06-12
TW338032B (en) 1998-08-11
DK0851850T3 (da) 2002-03-25
EA199800297A1 (ru) 1998-08-27
BR9610272A (pt) 1999-07-06
CZ76998A3 (cs) 1998-07-15
SK282779B6 (sk) 2002-12-03
SK32898A3 (en) 1998-11-04
AU6973896A (en) 1997-04-01
DE69617969T2 (de) 2002-06-27
DE69617969D1 (de) 2002-01-24
EP0851850B1 (en) 2001-12-12
RO120706B1 (ro) 2006-06-30
PT851850E (pt) 2002-05-31
ATE210624T1 (de) 2001-12-15
ES2167600T3 (es) 2002-05-16
CN1195337A (zh) 1998-10-07
EA001935B1 (ru) 2001-10-22
UA57001C2 (uk) 2003-06-16
HK1010189A1 (en) 1999-06-17

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