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ALKYL POLYAMINES HAVING A CYCLIC SUBSTITUENT METHODS OF PREPARING SUCH COMPOUNDS AND THEIR USE AS ANTIMICROBIALS

机译:具有循环取代法制备此类化合物的烷基多胺及其作为抗菌剂的用途

摘要

1499056 Dicycloalkylalkyl polyamines MERCK & CO Inc 22 April 1976 [28 April 1975] 16374/76 Heading C2C [Also in Divisions C5 and E1] The invention comprises compounds of the formula wherein A is cyclohexyl or cyclohexenyl which may be substituted by (C 1 -C 6 ) alkyl, each n is 0 or 1, R 1 is (C 1 -C 4 ) alkylene, Z is where Q is 1,4-piperidinediyl or -piperazinediyl; QSP1/SP is 1,4-cyclohexylene, R 2 is or (C 1 -C 4 )alkylene, R 3 is H, (C 1 -C 4 )alkyl, (C 2 -C 4 )aminoalkyl, (C 1 -C 4 )hydroxyalkyl or (C 2 -C 4 )dihydroxyalkyl, R 4 is or (C 1 -C 4 )alkylene, R 5 is H, H 2 N-CH 2 CH 2 -, H 2 N-CH 2 CH 2 CH 2 -, (C 1 -C 4 )monohydroxyalkyl, or (C 2 -C 4 )dihydroxyalkyl, R 6 is H, (C 1 -C 4 ) monohydroxyalkyl or (C 2 -C 4 )dihydroxyalkyl, R 7 and R 8 are direct links (C 1 -C 4 )- alkylene or -CH 2 CHOHCH 2 - radicals, and R 9 is aminoethyl, aminopropyl or aminohydroxypropyl; and acid addition salts thereof. They may be obtained by chemical or catalytic reduction of a Schiffs' base of the formula They are useful as antimicrobial agents and algae inhibitors. Antimicrobial compositions comprise compounds of the above formula together with a carrier. Ketones of the formula are obtained by acylative decarboxylation of acids of the formula at elevated temperature in the presence of transition metals or oxides thereof, alkaline earth metal oxides, polyphosphoric acid or BF 3 . Ketones of the above formula may also be obtained by a Grignard reaction of with a nitrile of the formula The acids of the above formula may be obtained by reacting an appropriate cyclohexene with an excess of refluxing aliphatic carboxylic acid anhydride in the presence of a free radicalforming catalyst. N - (3 - Aminopropyl) - 1,4 - cyclohexanebis- (methylamine) is obtained by reaction of acrylonitrile with 1,4-cyclohexane-bis(methylamine) followed by hydrogenation over a sponge Ni catalyst. N - (3 - Aminopropyl) - 1,4 - cyclohexane bis(2 - ethylamine); N,NSP1/SP - bis - (3- aminopropyl) - 1,4 - bis(2 - aminoethyl)cyclohexane, and N - (3 - aminopropyl) - NSP1/SP - (2- hydroxyethyl) - 1,4 - cyclohexanebis(methylamine) are obtained in a similar manner. N - (2 - Aminoethyl) - 1,4 - bis - (2 - aminoethyl) - cyclohexane is obtained by reacting 1,4-bis-(2-aminoethyl)cyclohexane with ethyleneimine. N - (2 - Hydroxyethyl) - 1,4 - bis - cyclohexanebis(methylamine is obtained by reacting 1,4- cyclohexanebis(methylamine) with ethylene oxide. N - (3 - Amino - 2 - hydroxypropyl) - 1,4 - cyclohexanebis(methylamine) and N - (2,3 - dihydroxypropyl) - 1,4 - cyclohexanebis(methylamine) are obtained by reacting 1,4 - cyclohexanebis- (methylamine) with epichlorohydrin and reacting propylene chlorohydrin obtained with NH 3 gas or aqueous methanolic NaOH respectively. N,N - Bis - (3 - hydroxypropyl) - 1,4 - cyclohexanebis(methylamine) is obtained by reacting 1 - bromomethyl - 4 - cyanocyclohexane with di - (3 - hydroxypropyl)amine and hydrogenating the resulting product over a sponge Ni catalyst. N,N - Di - (2,3 - dihydroxypropyl)trimethylenediamine is obtained by reacting bis-(2,3-dihydroxypropyl)amine with acrylonitrile and hydrogenating the resulting product as described above. The final product may be reacted with glycidol to form N,N,NSP1/SP-tri-(2,3- dihydroxypropyl)trimethylenediamine, which may in turn be reacted with acrylonitrile and the intermediate hydrogenated as above to give 5,9,9 - tri - (2,3 - dihydroxypropyl) - 1,5,9 - triazanonane.
机译:1499056二环烷基烷基多胺MERCK&CO Inc 1976年4月22日[1975年4月28日] 16374/76标题C2C [C5和E1处也存在]本发明包含下式的化合物,其中A为可被(C 1-取代的环己基或环己烯基C 6)烷基,每个n为0或1,R 1为(C 1 -C 4)亚烷基,Z为其中Q为1,4-哌啶二基或-哌嗪二基; Q 1 是1,4-亚环己基,R 2是或(C 1 -C 4)亚烷基,R 3是H,(C 1 -C 4)烷基,(C 2 -C 4)氨基烷基,(C 1 -C 4)羟烷基或(C 2 -C 4)二羟烷基,R 4为或(C 1 -C 4)亚烷基,R 5为H,H 2 N-CH 2 CH 2-,H 2 N-CH 2 CH 2 CH 2-,(C 1 -C 4)单羟基烷基或(C 2 -C 4)二羟基烷基,R 6为H,(C 1 -C 4)单羟基烷基或(C 2 -C 4) R 7和R 8是二羟基烷基,是直接连接的(C 1 -C 4)-亚烷基或-CH 2 CHOHCH 2-基,R 9是氨基乙基,氨基丙基或氨基羟丙基。及其酸加成盐。它们可以通过化学或催化还原下式的席夫斯碱获得。它们可用作抗微生物剂和藻类抑制剂。抗菌组合物包含上式的化合物以及载体。通过在高温下在过渡金属或其氧化物,碱土金属氧化物,多磷酸或BF 3的存在下,在高温下将式的酸进行酰基脱羧,可以得到式的酮。上式的酮也可以通过Grignard与下式的腈反应而制得。上式的酸可以通过使适当的环己烯与过量的回流脂肪族羧酸酐在自由基形成的条件下反应而制得。催化剂。通过使丙烯腈与1,4-环己烷-双(甲胺)反应,然后在海绵Ni催化剂上氢化,得到N-(3-氨基丙基)-1,4-环己烷双-(甲胺)。 N-(3-氨基丙基)-1,4-环己烷双(2-乙基胺); N,N 1 -双-(3-氨基丙基)-1,4-双(2-氨基乙基)环己烷和N-(3-氨基丙基)-N 1 -(2-羟乙基)-1,4-环己烷双(甲胺)以类似的方式获得。通过使1,4-双-(2-氨基乙基)环己烷与亚乙基亚胺反应,得到N-(2-氨基乙基)-1,4-双-(2-氨基乙基)-环己烷。 N-(2-羟基乙基)-1,4-双-环己烷双(甲胺)是通过使1,4-环己烷双(甲胺)与环氧乙烷反应制得的N-(3-氨基-2-羟丙基)-1,4-环己烷双通过使1,4-环己烷双-(甲胺)与环氧氯丙烷反应,并将得到的丙烯氯醇与NH 3气体或NaOH水溶液反应,制得(甲胺)和N-(2,3-二羟丙基)-1,4-环己烷双(甲胺)。 N,N-双-(3-羟丙基)-1,4-环己烷双(甲胺)是通过使1-溴甲基-4-氰基环己烷与二(3-羟丙基)胺反应并在海绵上氢化所得产物而获得的Ni催化剂,N,N-二-(2,3-二羟丙基)三亚甲基二胺是通过使双-(2,3-二羟丙基)胺与丙烯腈反应并如上所述氢化得到的产物而得到的,最终产物可以与缩水甘油反应。形成N,N,N 1 -三(2,3-二羟丙基)三亚甲基二胺ne,其可以依次与丙烯腈反应,并将中间体如上所述氢化,得到5,9,9-三-(2,3-二羟丙基)-1,5,9-三氮杂壬烷。

著录项

  • 公开/公告号GB1499056A

    专利类型

  • 公开/公告日1978-01-25

    原文格式PDF

  • 申请/专利权人 MERCK & CO INC;

    申请/专利号GB19760016374

  • 发明设计人

    申请日1976-04-22

  • 分类号C11D9/50;C07C87/38;C07C91/14;C07D295/12;C09K7/02;C11D3/48;E21B43/22;

  • 国家 GB

  • 入库时间 2022-08-22 21:39:59

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