RU2003100505A - METHOD FOR PRODUCING QUINOLINE DERIVATIVES - Google Patents

METHOD FOR PRODUCING QUINOLINE DERIVATIVES

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Publication number
RU2003100505A
RU2003100505A RU2003100505/04A RU2003100505A RU2003100505A RU 2003100505 A RU2003100505 A RU 2003100505A RU 2003100505/04 A RU2003100505/04 A RU 2003100505/04A RU 2003100505 A RU2003100505 A RU 2003100505A RU 2003100505 A RU2003100505 A RU 2003100505A
Authority
RU
Russia
Prior art keywords
formula
compound
amount
reaction mixture
water
Prior art date
Application number
RU2003100505/04A
Other languages
Russian (ru)
Other versions
RU2263110C2 (en
Inventor
Карл ШОЙЦГЕР
Original Assignee
Зингента Партисипейшнс Аг
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 Зингента Партисипейшнс Аг filed Critical Зингента Партисипейшнс Аг
Publication of RU2003100505A publication Critical patent/RU2003100505A/en
Application granted granted Critical
Publication of RU2263110C2 publication Critical patent/RU2263110C2/en

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Claims (2)

1. Способ получения соединения формулы I1. The method of obtaining the compounds of formula I
Figure 00000001
Figure 00000001
в которой R1 обозначает атом водорода или хлора, аin which R 1 represents a hydrogen or chlorine atom, and R2 обозначает атом водорода, C1-C8алкил или С18алкил, замещенный C18алкокси или С36алкенилокси, включающийR 2 represents a hydrogen atom, C 1 -C 8 alkyl or C 1 -C 8 alkyl substituted with C 1 -C 8 alkoxy or C 3 -C 6 alkenyloxy, including а) введение основной части от того количества соединения формулы IIa) the introduction of the main part of the amount of the compounds of formula II
Figure 00000002
Figure 00000002
которое должно взаимодействовать, в смесь растворителей, включающую по меньшей мере один органический растворитель, способный образовывать с водой азеотроп, и по меньшей мере один апротонный биполярный растворитель;which must interact in a solvent mixture comprising at least one organic solvent capable of forming an azeotrope with water and at least one aprotic bipolar solvent; б) дозирование в водное сильное основание, взятое в количестве, эквивалентном основной части общего количества этого соединения формулы II;b) dosing into an aqueous strong base, taken in an amount equivalent to the main part of the total amount of this compound of formula II; в) добавление оставшейся части от того количества соединения формулы II, которое должно взаимодействовать;c) adding the remainder of the amount of the compound of formula II to be reacted; г) добавление слабого основания в количестве, которое по меньшей мере эквивалентно этой оставшейся части;g) adding a weak base in an amount that is at least equivalent to this remaining part; д) удаление воды из реакционной смеси азеотропной дистилляцией;d) removing water from the reaction mixture by azeotropic distillation; е) добавление соединения формулы IIIe) adding a compound of formula III
Figure 00000003
Figure 00000003
в которой R2 имеет такие же значения, как указанные для формулы I; иin which R 2 has the same meanings as indicated for formula I; and ж) выделение из реакционной смеси полученного соединения формулы 1.g) isolation from the reaction mixture of the obtained compound of formula 1.
2. Способ по п.1, в котором соединение формулы I выделяют из реакционной смеси после завершения реакционной стадии е) отгонкой растворителей из расплава продукта, экстракцией расплава продукта водой, а затем удалением из расплава продукта водной фазы.2. The method according to claim 1, in which the compound of formula I is isolated from the reaction mixture after completion of the reaction step e) by distilling off the solvents from the product melt, extracting the product melt with water, and then removing the aqueous phase from the product melt.
RU2003100505/04A 2000-06-28 2001-06-26 Method for preparing derivatives of quinoline RU2263110C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH12742000 2000-06-28
CH1274/00 2000-06-28

Publications (2)

Publication Number Publication Date
RU2003100505A true RU2003100505A (en) 2004-06-27
RU2263110C2 RU2263110C2 (en) 2005-10-27

Family

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RU2003100505/04A RU2263110C2 (en) 2000-06-28 2001-06-26 Method for preparing derivatives of quinoline

Country Status (23)

Country Link
US (1) US6660865B2 (en)
EP (1) EP1294694B1 (en)
JP (1) JP3955814B2 (en)
KR (1) KR100572818B1 (en)
CN (1) CN1256327C (en)
AR (1) AR029283A1 (en)
AT (1) ATE280760T1 (en)
AU (1) AU780534B2 (en)
BR (2) BRPI0112064B8 (en)
CA (1) CA2412543C (en)
DE (1) DE60106760T2 (en)
DK (1) DK1294694T3 (en)
ES (1) ES2228923T3 (en)
HU (1) HU230214B1 (en)
IL (2) IL153424A0 (en)
MX (1) MXPA02012398A (en)
PL (1) PL200447B1 (en)
PT (1) PT1294694E (en)
RU (1) RU2263110C2 (en)
TW (1) TWI230154B (en)
UA (1) UA73587C2 (en)
WO (1) WO2002000625A2 (en)
ZA (1) ZA200300328B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102239149B (en) * 2008-10-06 2015-05-13 约翰·霍普金斯大学 Quinoline compounds as inhibitors of angiogenesis, human methionine aminopeptidase, and sirt1, and methods of treating disorders
CN101805288A (en) * 2010-04-21 2010-08-18 新沂市永诚化工有限公司 Novel method for synthesizing cloquintocet-mexyl
GB201119690D0 (en) 2011-11-14 2011-12-28 Syngenta Participations Ag Process for the preparation of compounds
CN102718706B (en) * 2012-05-31 2014-05-07 绍兴文理学院 Preparation method for 2-(5-chlorine-8-quinoline oxygen group) acetic acid
CN103524411B (en) * 2013-10-21 2015-03-04 哈尔滨理工大学 Synthetic method of 5-cholro-8-quinoline oxyacetic acid
CN105001158B (en) * 2015-07-09 2018-02-02 北京颖泰嘉和生物科技股份有限公司 A kind of method for synthesizing cloquitocet_mexyl
CN113135851B (en) * 2021-04-26 2024-10-01 甘肃联凯生物科技有限公司 Synthesis method of cloquintocet-mexyl

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3382743D1 (en) * 1982-05-07 1994-05-11 Ciba Geigy Use of quinoline derivatives to protect crops.
EP0492366B1 (en) * 1990-12-21 1997-03-26 Hoechst Schering AgrEvo GmbH New 5-chloroquinolin-8-oxyalkanecarbonic acid derivatives, process for their preparation and their use as antidotes for herbicides

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