KR840006216A - Method for preparing 2-alkyl-4-amino-5-aminomethylpyrimidine - Google Patents

Method for preparing 2-alkyl-4-amino-5-aminomethylpyrimidine Download PDF

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KR840006216A
KR840006216A KR1019830003442A KR830003442A KR840006216A KR 840006216 A KR840006216 A KR 840006216A KR 1019830003442 A KR1019830003442 A KR 1019830003442A KR 830003442 A KR830003442 A KR 830003442A KR 840006216 A KR840006216 A KR 840006216A
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South Korea
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ammonia
amino
alkyl
formylpyrimidine
reaction
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KR1019830003442A
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Korean (ko)
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KR900001197B1 (en
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고오조오 후지이 (외 1)
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미즈노 가즈오
우베고오산 가부시끼가이샤
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Priority claimed from JP57154661A external-priority patent/JPS5944364A/en
Priority claimed from JP15891682A external-priority patent/JPS5948464A/en
Application filed by 미즈노 가즈오, 우베고오산 가부시끼가이샤 filed Critical 미즈노 가즈오
Publication of KR840006216A publication Critical patent/KR840006216A/en
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Publication of KR900001197B1 publication Critical patent/KR900001197B1/en

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    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음No content

Description

2-알킬-4-아미노-5-아미노메틸피리미딘의 제조방법Method for preparing 2-alkyl-4-amino-5-aminomethylpyrimidine

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (14)

2-알킬-4-아미노-5-포르밀피리미딘을 환원촉매의 존재하에 수소 및 암모니아와 촉매반응시킴을 특징으로하는 2-알킬-4-아미노-5-아미노메틸피리미딘의 제조방법.A process for preparing 2-alkyl-4-amino-5-aminomethylpyrimidine characterized by catalyzing 2-alkyl-4-amino-5-formylpyrimidine with hydrogen and ammonia in the presence of a reducing catalyst. 제1항에 있어서, 2가 니켈의 염을 환원촉매에 추가하여 반응계에 도입함을 특징으로 하는 제조방법.The method according to claim 1, wherein a salt of divalent nickel is added to the reaction system in addition to a reduction catalyst. 제2항에 있어서, 2가 니켈의 염을 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 0.1 내지 5몰 사용함을 특징으로 하는 제조방법.The process according to claim 2, wherein a salt of divalent nickel is used at 0.1 to 5 moles per mole of 2-alkyl-4-amino-5-formylpyrimidine. 제1항 또는 제2항에 있어서, 2-알킬-4-아미노-5-포르밀피리미딘을 불활성용제중에서 암모니아와 반응시키는 과정과, 그렇게 얻어진 반응생성물을 환원시키기 위해 이 반응생성물을 반응혼합물로부터 단리시키지 않은 그대로 암모니아, 수소 및 환원촉매를 함유하고 있는 불활성용제에 가하는 과정으로 되어있는 것을 특징으로 하는 제조방법.The process of claim 1 or 2, wherein the reaction product is reacted with ammonia in an inert solvent and the reaction product is reduced from the reaction mixture to reduce the reaction product thus obtained. A process for producing a non-isolated, inert solvent containing ammonia, hydrogen and a reducing catalyst. 제1항 또는 제2항에 있어서, 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 5 내지 400몰의 수소를 사용하는 것을 특징으로 하는 제조방법.The process according to claim 1 or 2, wherein 5 to 400 moles of hydrogen are used per mole of 2-alkyl-4-amino-5-formylpyrimidine. 제1항 또는 제2항에 있어서, 환원촉매는 팔라듐, 로듐, 백금, 루테늄, 니켈, 코발트, 철, 구리 및 크롬으로된 군으로부터 선택한 금속원자를 함유하고 있고, 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 금속으로서 0.001 내지 3그램 원자의 양으로 사용되는 것을 특징으로 하는 제조방법.The catalyst according to claim 1 or 2, wherein the reduction catalyst contains a metal atom selected from the group consisting of palladium, rhodium, platinum, ruthenium, nickel, cobalt, iron, copper and chromium, and 2-alkyl-4-amino- A method according to claim 1, wherein the metal is used per mole of 5-formylpyrimidine in an amount of 0.001 to 3 gram atoms. 제1항 또는 제2항에 있어서, 0 내지 200℃의 온도에서 촉매반응을 행하는 것을 특징으로 하는 제조방법.The process according to claim 1 or 2, wherein the reaction is carried out at a temperature of 0 to 200 캜. 제1항 또는 제2항에서 있어서, 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 4 내지 500몰의 양으로 액체암모니아, 암모니아기체 및 암모니아수의 형태로 암모니아를 사용하는 것을 특징으로하는 제조방법.3. Ammonia according to claim 1 or 2, characterized in that ammonia is used in the form of liquid ammonia, ammonia gas and ammonia water in an amount of 4 to 500 moles per mole of 2-alkyl-4-amino-5-formylpyrimidine. Manufacturing method. 제4항에 있어서, 2-알킬-4-아미노-5-포르밀피리미딘과의 반응을 위한 암모니아를 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 4 내지 500몰의 양으로 액체암모니아, 암모니아기체 또는 암모니아수의 형태로 사용하는 것을 특징으로 하는 제조방법.The amount of 4 to 500 moles per mole of 2-alkyl-4-amino-5-formylpyrimidine according to claim 4, wherein the ammonia for reaction with 2-alkyl-4-amino-5-formylpyrimidine is added. To a liquid ammonia, ammonia gas or ammonia water. 제4항에 있어서, 2-알킬-4-아미노-5-포르밀피리미딘과 암모니아와의 반응을 위한 용제를 2-알킬-4-아미노-5-포르밀피리미딘의 1중량부당 3 내지 30중량부의 양으로 사용하는 것을 특징으로 하는 제조방법.The solvent for reaction of 2-alkyl-4-amino-5-formylpyrimidine with ammonia is 3 to 30 per 1 part by weight of 2-alkyl-4-amino-5-formylpyrimidine. A production method characterized by the use of the amount by weight. 제4항에 있어서, 2-알킬-4-아미노-5-포르밀피리미딘과 암모니아와의 반응을 0 내지 130℃온도에서 1 내지 100kg/㎠G의 암모니아분압하에서 행하는 것을 특징으로 하는 제조방법.The production process according to claim 4, wherein the reaction between 2-alkyl-4-amino-5-formylpyrimidine and ammonia is performed at an ammonia partial pressure of 1 to 100 kg / cm 2 G at a temperature of 0 to 130 ° C. 제1항 또는 제2항에 있어서, 촉매반응을 0 내지 200℃의 온도에서 행하는 것을 특징으로 하는 제조방법.The production process according to claim 1 or 2, wherein the catalytic reaction is carried out at a temperature of 0 to 200 캜. 제4항에 있어서, 촉매반응을 위한 암모니아를 2-알킬-4-아미노-5-포르밀피리미딘의 1몰당 4 내지 300몰의 양으로 액체암모니아, 암모니아기체 및 암모니아수의 형태로 사용하는 것을 특징으로 하는 제조방법.Ammonia for catalysis is used in the form of liquid ammonia, ammonia gas and ammonia water in an amount of 4 to 300 moles per mole of 2-alkyl-4-amino-5-formylpyrimidine. The manufacturing method to make. 제4항에 있어서, 촉매반응을 위한 촉매를 2-알킬-4-아미노-5-포르밀피리미딘의 1중량부당 2 내지 20중량부의 양으로 사용하는 것을 특징으로 하는 제조방법.The process according to claim 4, wherein the catalyst for catalysis is used in an amount of 2 to 20 parts by weight per 1 part by weight of 2-alkyl-4-amino-5-formylpyrimidine. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019830003442A 1982-09-07 1983-07-25 Process for preparing 2-alkyl-4-amino-5-aminomethyl pyrimidine KR900001197B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP57154661A JPS5944364A (en) 1982-09-07 1982-09-07 Preparation of 2-lakyl-4-amino-5-aminomethylpyrimidine
JP57-154661 1982-09-07
JP15891682A JPS5948464A (en) 1982-09-14 1982-09-14 Preparation of 2-alkyl-4-amino-5-aminomethylpyrimidine
JP57-158916 1982-09-14

Publications (2)

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KR840006216A true KR840006216A (en) 1984-11-22
KR900001197B1 KR900001197B1 (en) 1990-02-28

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KR1019830003442A KR900001197B1 (en) 1982-09-07 1983-07-25 Process for preparing 2-alkyl-4-amino-5-aminomethyl pyrimidine

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KR (1) KR900001197B1 (en)
DK (1) DK156723C (en)
HU (1) HU190727B (en)
IT (1) IT1173749B (en)

Also Published As

Publication number Publication date
DK156723C (en) 1990-02-19
DK156723B (en) 1989-09-25
IT8348764A0 (en) 1983-07-27
HU190727B (en) 1986-10-28
KR900001197B1 (en) 1990-02-28
IT1173749B (en) 1987-06-24
DK342283D0 (en) 1983-07-26
DK342283A (en) 1984-03-08

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