CH235236A - Process for the preparation of 2 ', 3', 5'-trimethyl-cyclopentane-1 ', 5-spiro-1-methyl-2,4,6-triketo-hexahydropyrimidine. - Google Patents

Process for the preparation of 2 ', 3', 5'-trimethyl-cyclopentane-1 ', 5-spiro-1-methyl-2,4,6-triketo-hexahydropyrimidine.

Info

Publication number
CH235236A
CH235236A CH235236DA CH235236A CH 235236 A CH235236 A CH 235236A CH 235236D A CH235236D A CH 235236DA CH 235236 A CH235236 A CH 235236A
Authority
CH
Switzerland
Prior art keywords
sep
methyl
spiro
hexahydropyrimidine
triketo
Prior art date
Application number
Other languages
German (de)
Inventor
Ag J R Geigy
Original Assignee
Ag J R Geigy
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 Ag J R Geigy filed Critical Ag J R Geigy
Publication of CH235236A publication Critical patent/CH235236A/en

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Description

  

  Verfahren zur Herstellung von     2',3',5'-Trimethyl-eyelopentan-1',5-spiro-l-methyl-          2,4,6-tr        iketo-hegahydropyr        imidin.     
EMI0001.0005     
  
    Gegenstand <SEP> vorliegenden <SEP> Zusatzpatentes
<tb>  iGt <SEP> :ein <SEP> Verfahren <SEP> zur <SEP> Herstellung <SEP> von
<tb>  2',3', <SEP> 5' <SEP> - <SEP> Trilmethyl <SEP> - <SEP> cyelloipentan@-, <SEP> 1', <SEP> 5 <SEP> - <SEP> sl)iro,-1  methyl <SEP> - <SEP> 2,4,6 <SEP> - <SEP> triketo <SEP> - <SEP> hexahydropyrimi-diin,
<tb>  welzhea <SEP> dadurch <SEP> gekennzeichnet <SEP> ist, <SEP> dass <SEP> man
<tb>  2, <SEP> 3, <SEP> 5-Tri@m!ethyl <SEP> - <SEP> cyclopentan-l-cyan-1-oarbon  sä.ureester <SEP> mit <SEP> Methyiha:

  rnstoff <SEP> kondensiert
<tb>  und <SEP> das <SEP> erhaltene <SEP> Produkt <SEP> anschliessend <SEP> der
<tb>  Hydfrolyse <SEP> unterwirft.
<tb>  



  Die <SEP> neue <SEP> Verbindung <SEP> ist <SEP> ein <SEP> ho:ch.visk <SEP> oses,
<tb>  schwach <SEP> gelblich <SEP> gefärbtes <SEP> 01, <SEP> Kp.,)" <SEP> 139 <SEP> bis
<tb>  141 . <SEP> Sie <SEP> beeitzt <SEP> na-rkotisehe <SEP> Wirkung.
<tb>  



  <I>Bespiel:</I>
<tb>  Zu <SEP> einer <SEP> Lösung <SEP> von <SEP> 4,6 <SEP> Teilen <SEP> Natrium
<tb>  in <SEP> 70 <SEP> T'ei,len <SEP> ab@solutern <SEP> Alkohol <SEP> fügt <SEP> man
<tb>  20,9 <SEP> Teile <SEP> 2,3,5-Trimethyl-cyclopentan-l  cyan-1-carbans@äureäthyleisteir <SEP> und <SEP> 7 <SEP> Teile
<tb>  Meithylbfarnstoff <SEP> und <SEP> erhitzt <SEP> 10 <SEP> Stunden <SEP> lang
<tb>  untrer <SEP> Rückflussikühlung. <SEP> Hierauf <SEP> destilliert
<tb>  mann <SEP> den <SEP> Alkohol <SEP> ab <SEP> und <SEP> erhitzt <SEP> den <SEP> Rück-     
EMI0001.0006     
  
    ,stand <SEP> mit <SEP> der <SEP> 66:e:

  chsfachen <SEP> Menge <SEP> Schwefel  säure <SEP> (25%ig) <SEP> 8 <SEP> .Stunden, <SEP> lang <SEP> zum <SEP> Sieden.
<tb>  Die <SEP> neue <SEP> Verbindung <SEP> lä@sst <SEP> ,sich <SEP> nicht <SEP> im. <SEP> kri  stallisiemter <SEP> Form <SEP> erhalten, <SEP> sie <SEP> wird <SEP> durch
<tb>  Ausäthern <SEP> isoliert <SEP> und <SEP> nach <SEP> dem <SEP> Trocknen
<tb>  über <SEP> entwässertem <SEP> Natriumsulfat <SEP> und <SEP> Ver  jagen <SEP> des <SEP> Äthers <SEP> im <SEP> Vakuum <SEP> destilliert.



  Process for the preparation of 2 ', 3', 5'-trimethyl-eyelopentan-1 ', 5-spiro-1-methyl-2,4,6-triketo-hegahydropyrimidine.
EMI0001.0005
  
    Subject <SEP> of the present <SEP> additional patent
<tb> iGt <SEP>: a <SEP> process <SEP> for <SEP> production <SEP> of
<tb> 2 ', 3', <SEP> 5 '<SEP> - <SEP> Trilmethyl <SEP> - <SEP> cyelloipentan @ -, <SEP> 1', <SEP> 5 <SEP> - <SEP> sl) iro, -1 methyl <SEP> - <SEP> 2,4,6 <SEP> - <SEP> triketo <SEP> - <SEP> hexahydropyrimi-diyne,
<tb> welzhea <SEP> characterized by <SEP> <SEP>, <SEP> that <SEP> man
<tb> 2, <SEP> 3, <SEP> 5-Tri @ m! ethyl <SEP> - <SEP> cyclopentane-1-cyano-1-carbonic acid ester <SEP> with <SEP> Methyiha:

  substance <SEP> condensed
<tb> and <SEP> the <SEP> received <SEP> product <SEP> then <SEP> the
<tb> Subject to hydrolysis <SEP>.
<tb>



  The <SEP> new <SEP> connection <SEP> is <SEP> a <SEP> ho: ch.visk <SEP> oses,
<tb> weak <SEP> yellowish <SEP> colored <SEP> 01, <SEP> Kp.,) "<SEP> 139 <SEP> to
<tb> 141. <SEP> You <SEP> mitzt <SEP> na-rkotisehe <SEP> effect.
<tb>



  <I> Example: </I>
<tb> To <SEP> a <SEP> solution <SEP> of <SEP> 4.6 <SEP> parts <SEP> sodium
<tb> in <SEP> 70 <SEP> parts <SEP> from @ solutern <SEP> alcohol <SEP> adds <SEP> man
<tb> 20.9 <SEP> parts <SEP> 2,3,5-trimethyl-cyclopentane-1 cyan-1-carbans @ äureäthyleisteir <SEP> and <SEP> 7 <SEP> parts
<tb> Meithylbfarnstoff <SEP> and <SEP> heated <SEP> for 10 <SEP> hours <SEP>
<tb> under <SEP> reflux cooling. <SEP> Then <SEP> distilled
<tb> man <SEP> heats <SEP> alcohol <SEP> from <SEP> and <SEP> <SEP> the <SEP> return
EMI0001.0006
  
    , stood <SEP> with <SEP> the <SEP> 66: e:

  xfold <SEP> amount <SEP> sulfuric acid <SEP> (25%) <SEP> 8 <SEP>. hours, <SEP> long <SEP> for <SEP> boiling.
<tb> The <SEP> new <SEP> connection <SEP> leaves <SEP>, <SEP> not <SEP> in. <SEP> crystallized <SEP> form <SEP> received, <SEP> it <SEP> becomes <SEP>
<tb> Ethering <SEP> isolates <SEP> and <SEP> after <SEP> the <SEP> drying
<tb> over <SEP> dehydrated <SEP> sodium sulfate <SEP> and <SEP> expelling <SEP> the <SEP> ether <SEP> distilled in the <SEP> vacuum <SEP>.

 

Claims (1)

EMI0001.0007 PATENTANSPRUCH: <tb> Verfahren. <SEP> zur <SEP> Herstellung <SEP> von <SEP> 2',3',5' Triimeithyl-eycl:opentan-1',5 <SEP> -,spiro-1-methyl 2,4,6-t,rik@eto-hexahydropyrimidin, <SEP> dadurch <tb> gekennzeichnet, <SEP> dass <SEP> man <SEP> 2,3,5-Trim:ethyl cycl.opent9,n-1-cyan <SEP> - <SEP> 1- <SEP> carbonsäuree.ster <SEP> mit <tb> Methylharn!srtaff <SEP> kon:densien-t <SEP> und <SEP> das <SEP> erhal tene <SEP> Produkt <SEP> anschliessend <SEP> der <SEP> Hydrolyse <SEP> un terwirft. <tb> Die <SEP> neue <SEP> Verbindung <SEP> ist <SEP> ein <SEP> hochviskoses, <tb> schwach <SEP> gelblich <SEP> gefärbteo <SEP> 01, <SEP> Kp. <SEP> 0,4 <SEP> 139 <SEP> bis <tb> 14l . <SEP> Sie <SEP> besitzt <SEP> narkotische <SEP> Wirkung. EMI0001.0007 PATENT CLAIM: <tb> procedure. <SEP> for <SEP> production <SEP> of <SEP> 2 ', 3', 5 'Triimeithyl-eycl: opentan-1', 5 <SEP> -, spiro-1-methyl 2,4,6-t , rik @ eto-hexahydropyrimidine, <SEP> thereby <tb> marked, <SEP> that <SEP> man <SEP> 2,3,5-trim: ethyl cycl.opent9, n-1-cyan <SEP> - <SEP> 1- <SEP> carbonsäuree.ster < SEP> with <tb> methyl urine! srtaff <SEP> kon: densien-t <SEP> and <SEP> the <SEP> received <SEP> product <SEP> then <SEP> subjected to the <SEP> hydrolysis <SEP>. <tb> The <SEP> new <SEP> connection <SEP> is <SEP> a <SEP> highly viscous, <tb> weak <SEP> yellowish <SEP> colored o <SEP> 01, <SEP> Kp. <SEP> 0.4 <SEP> 139 <SEP> to <tb> 14l. <SEP> You <SEP> has <SEP> narcotic <SEP> effect.
CH235236D 1942-07-29 1942-07-29 Process for the preparation of 2 ', 3', 5'-trimethyl-cyclopentane-1 ', 5-spiro-1-methyl-2,4,6-triketo-hexahydropyrimidine. CH235236A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH235236T 1942-07-29
CH230367T 1942-07-29

Publications (1)

Publication Number Publication Date
CH235236A true CH235236A (en) 1944-11-15

Family

ID=25727475

Family Applications (1)

Application Number Title Priority Date Filing Date
CH235236D CH235236A (en) 1942-07-29 1942-07-29 Process for the preparation of 2 ', 3', 5'-trimethyl-cyclopentane-1 ', 5-spiro-1-methyl-2,4,6-triketo-hexahydropyrimidine.

Country Status (1)

Country Link
CH (1) CH235236A (en)

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