CN1089339C - 4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的制备 - Google Patents

4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的制备 Download PDF

Info

Publication number
CN1089339C
CN1089339C CN96192517A CN96192517A CN1089339C CN 1089339 C CN1089339 C CN 1089339C CN 96192517 A CN96192517 A CN 96192517A CN 96192517 A CN96192517 A CN 96192517A CN 1089339 C CN1089339 C CN 1089339C
Authority
CN
China
Prior art keywords
amino
dimethoxy
solvent
temperature
preparation
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
CN96192517A
Other languages
English (en)
Chinese (zh)
Other versions
CN1178526A (zh
Inventor
J·J·罗卡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of CN1178526A publication Critical patent/CN1178526A/zh
Application granted granted Critical
Publication of CN1089339C publication Critical patent/CN1089339C/zh
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
CN96192517A 1995-03-14 1996-03-07 4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的制备 Expired - Lifetime CN1089339C (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/404,215 US5523405A (en) 1995-03-14 1995-03-14 Preparation of 4,6-dimethoxy-2-((phenoxycarbonyl)amino)-pyrimidine
US08/404,215 1995-03-14

Publications (2)

Publication Number Publication Date
CN1178526A CN1178526A (zh) 1998-04-08
CN1089339C true CN1089339C (zh) 2002-08-21

Family

ID=23598652

Family Applications (1)

Application Number Title Priority Date Filing Date
CN96192517A Expired - Lifetime CN1089339C (zh) 1995-03-14 1996-03-07 4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的制备

Country Status (19)

Country Link
US (1) US5523405A (enExample)
EP (1) EP0815086B1 (enExample)
JP (1) JP3862751B2 (enExample)
KR (1) KR100392869B1 (enExample)
CN (1) CN1089339C (enExample)
AU (1) AU5173496A (enExample)
BR (1) BR9607860A (enExample)
CA (1) CA2215202A1 (enExample)
CZ (1) CZ288397A3 (enExample)
DE (1) DE69605105T2 (enExample)
EA (1) EA199800090A1 (enExample)
ES (1) ES2140835T3 (enExample)
HU (1) HUP9801329A3 (enExample)
IL (1) IL117433A (enExample)
IN (1) IN180379B (enExample)
PL (1) PL322178A1 (enExample)
TW (1) TW382011B (enExample)
WO (1) WO1996028428A1 (enExample)
ZA (1) ZA962066B (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009062542A1 (de) * 2007-11-13 2009-05-22 Osram Gesellschaft mit beschränkter Haftung Schaltungsanordnung und verfahren zum betreiben einer hochdruckentladungslampe
CN101423499B (zh) * 2008-12-12 2010-12-29 江苏工业学院 高纯4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶制备方法
DE202009011727U1 (de) 2009-08-28 2009-12-17 Osram Gesellschaft mit beschränkter Haftung Entladungslampe mit Reflektor
CN103848791B (zh) * 2014-03-19 2015-09-09 北京英力精化技术发展有限公司 一种4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的合成方法
CN111423385B (zh) * 2020-05-22 2022-02-18 北京英力精化技术发展有限公司 4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的精制方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5017212A (en) * 1986-03-20 1991-05-21 Takeda Chemical Industries, Ltd. Sulfonylurea compounds and herbicidal use
DE4241303A1 (de) * 1992-12-08 1994-06-09 Bayer Ag Substituierte Chinolylsulfonylharnstoffe

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102444A (en) * 1986-12-08 1992-04-07 E. I. Du Pont De Nemours And Company Herbicidal pyridinesulfonylureas

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5017212A (en) * 1986-03-20 1991-05-21 Takeda Chemical Industries, Ltd. Sulfonylurea compounds and herbicidal use
DE4241303A1 (de) * 1992-12-08 1994-06-09 Bayer Ag Substituierte Chinolylsulfonylharnstoffe

Also Published As

Publication number Publication date
KR100392869B1 (ko) 2003-10-17
US5523405A (en) 1996-06-04
ZA962066B (en) 1997-11-26
IL117433A0 (en) 1996-07-23
DE69605105T2 (de) 2000-05-25
AU5173496A (en) 1996-10-02
CZ288397A3 (cs) 1999-01-13
ES2140835T3 (es) 2000-03-01
EA199800090A1 (ru) 1998-08-27
KR19980703064A (ko) 1998-09-05
BR9607860A (pt) 1998-06-30
TW382011B (en) 2000-02-11
HUP9801329A3 (en) 1998-12-28
HUP9801329A2 (hu) 1998-10-28
DE69605105D1 (de) 1999-12-16
JPH11501919A (ja) 1999-02-16
IL117433A (en) 2000-02-17
CA2215202A1 (en) 1996-09-19
PL322178A1 (en) 1998-01-19
IN180379B (enExample) 1998-01-24
JP3862751B2 (ja) 2006-12-27
EP0815086B1 (en) 1999-11-10
EP0815086A1 (en) 1998-01-07
MX9706972A (es) 1997-11-29
CN1178526A (zh) 1998-04-08
WO1996028428A1 (en) 1996-09-19

Similar Documents

Publication Publication Date Title
CN1089339C (zh) 4,6-二甲氧基-2-((苯氧基羰基)氨基)-嘧啶的制备
DE69910799T2 (de) Als inhibitoren der aicarftnützliche verbindungen
KR100344115B1 (ko) 1-치환된-5(4h)-테트라졸리논의제조방법
JPH10120659A (ja) 3−アリール−ウラシルの製法
JP3536217B2 (ja) グアニジン誘導体の製造方法
JP3512844B2 (ja) 1−アミノ−1−シアナミド−2,2−ジシアノエチレン ナトリウム塩の製造方法
RU2156238C2 (ru) Способ получения диоксоазабициклогексанов
JPS6272662A (ja) 4−アルコキシ−3−ピロリン−2−オン−1−イル−酢酸アルキルエステルおよびその製造方法
JP2991832B2 (ja) ピリミジン誘導体の製造方法
MXPA97006972A (en) Preparation of 4,6-dimetoxy-2 - ((fenoxicarbonil) amino) -pirimid
JPS6125026B2 (enExample)
CN1436177A (zh) 制备取代的5-氨基-n-苯基-1,2,4-三唑-3-磺酰胺的方法
JP3042123B2 (ja) N−シアノアセトアミジン誘導体の製法
JPH07291917A (ja) アシルイソシアネート類の製造方法
SU1735296A1 (ru) Способ получени 1-(2 @ ,4 @ ,6 @ -трихлорфенил)-3-(2 @ -хлор-5 @ -октадецилсукцинимидофениламино)-4-(1 @ -нафтилазо)пиразолона-5 @
JPH09124569A (ja) ベンズアミド誘導体の製造方法
JPH04182465A (ja) N―メトキシ―n―メチルアミノアルキルフタルイミドの製造法
CN101048387A (zh) 苯基2-嘧啶酮及其新的中间体的制备方法
JPH08217743A (ja) 2,6−ジイソプロピルフェニルカルボジイミドの精製法
JPWO2002085880A1 (ja) ニトリル化合物の製造方法
JPH0344375A (ja) 5―ヒドロキシピラゾール類の製造法
JPH08208579A (ja) 1−アミノ−5−ベンゾイルアミノアントラキノンの製造法
JPS63122680A (ja) 結晶性2―(1―ペンチル―3―グアニジノ)―4―(2―メチル―4―イミダゾリル)チアゾール・二塩酸塩・三水和物
WO1995021828A1 (en) Process for producing hexahydropyridazine and hexahydropyridazine-1,2-dicarboxylate derivative
JP2003040855A (ja) 含フッ素コハク酸系化合物の固液分離可能な晶析方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
CX01 Expiry of patent term

Granted publication date: 20020821

EXPY Termination of patent right or utility model