首页> 外国专利> DIFFERENTIAL MOBILITY OF COLOR MOIETY IN COLOR TRANSFER

DIFFERENTIAL MOBILITY OF COLOR MOIETY IN COLOR TRANSFER

机译:颜色转移中颜色部分的微分流动性

摘要

1,243,048. Azo and anthraquinone dyes. INTERNATIONAL POLAROID' CORP. 23 July; 1968 [24 July, 1967], No. 1734/71 Divided out of 1,243,045. Heading C4P. [Also in Division C2] Mono-azo, dis-azo or anthraquinone dyes for photographic transfer processes are-of formula wherein A represents the atoms necessary to complete a benzene or naphthalene radical that may be further substituted; D is a monoazo, disazo or anthraquinone colour providing moiety, Z is hydrogen, chloro, bromo, carboxy sulpho, hydroxy, alkoxy, hydroxyalkyl, or an aromatic amino radical unsubstituted ortho to said amino group; Y is the residue'of an acid group forming an amide with and reducing the basic character of the nitrogen atom to which it is bonded; X is hydroxy; or when Z is an anilino or naphthylamino radical containing, a y-amino or p-hydroxy substituent but unsubstituted ortho to said amino group joined to the ring completed by A, X may also be hydrogen or a primary, secondary or tertiary amino group or an alkyl, aromatic or heterpcyclic substituent; RSP1/SP is hydrogen, alkyl, cycloalkyl or substituted alkyl, and wherein the values of A, X, Z and RSP1/SP are such that the compound is non-diffusible in alkaline photographic processing solution. The examples describe (1) reacting (2- hydroxy - 4 - amine-HCl - 5 - chloro - 4SP1 /SP- carbon-dodecylamide) diphenyl and 4- (2-naphthol- 1 - azo) benzene sulphonyl chloride (A) to form a dye of Formula (I) (2) reacting N'-(o-aminophenyl)-4-methoxy-3- (NSP1/SP,-dodecylamidoethyl) aniline (B) and sulphonyl chloride (A) to form a dye of Formula (XIX) (3) repeating (2) but using an octadecamido compound to form a dye of Formula (XX) (4) reacting diazotized sulphanilic and 1-phenyl- 3. - carbethoxy - pyrazolone - 5 to form 1- phenyl - 3 - carbethoxy - 4 - (p -,'ulphophenylaze)- pyrazolone-5 sodium salt which,is reacted with propylamine to form the corresponding 3-propylamido compound which is reacted with thionyl chloride to form the corresponding pchlorosulphonylphenylazo compound which is reacted with compound (B) to form a methoxy compound which is demethylated with BBr 3 to form a due of Formula (XXI) (5) 2 - amino - 4 - stearylamide. - N - (41.- methoxy - 3SP1 /SP- carboxyphenyl) aniline is reacted with 4SP1/SP - (sulphonylchloride) - phenylazo - 2 - naphthol to form a methoxy compound which is demethylated to a dye of Formula (XVI).
机译:1,243,048。偶氮和蒽醌染料。 INTERNATIONAL POLAROID'CORP。7月23日; 1968年[1967年7月24日],第1734/71号,从1,243,045中分割。标题C4P。 [也在C2部分中]用于照相转印方法的单偶氮,双偶氮或蒽醌染料具有下式:其中A表示完成可以被进一步取代的苯或萘基所必需的原子; D为提供单偶氮,二偶氮或蒽醌的颜色部分,Z为氢,氯,溴,羧基磺基,羟基,烷氧基,羟烷基或在所述氨基附近未取代的芳族氨基。 Y是形成酰胺并与之键合的氮原子的碱性降低的酰胺基的酸基的残基。 X是羟基;或当Z为含有苯氨基或对羟基取代基但未取代的邻氨基或对氨基的萘基时,所述氨基与由A完成的环相连,X也可以是氢或伯,仲或叔氨基或烷基,芳族或杂环取代基; R 1 是氢,烷基,环烷基或取代的烷基,并且其中A,X,Z和R 1 的值使得该化合物在碱性下不可扩散摄影冲洗液。实施例描述了(1)使(2-羟基-4-胺-HCl-5-氯-4 1 -碳十二烷基酰胺)二苯基与4-(2-萘酚-1-偶氮)苯反应磺酰氯(A)形成与N'-(邻氨基苯基)-4-甲氧基-3-(N 1 ,-十二烷基酰胺基乙基)苯胺反应的染料(I)(B) )和磺酰氯(A)形成重复(2)的式(XIX)(3)的染料,但使用十八碳酰胺基化合物形成式(XX)(4)的染料,使重氮化的磺胺基化合物和1-苯基-3反应。 -甲乙氧基-吡唑啉酮-5形成1-苯基-甲乙氧基--4-(对-,'ulphophenylaze)-吡唑啉酮-5钠盐,其与丙胺反应形成相应的3-丙基酰胺基化合物,其与亚硫酰反应氯化物形成相应的对氯磺酰基苯基偶氮化合物,该化合物与化合物(B)反应形成甲氧基化合物,该甲氧基化合物用BBr 3脱甲基形成通式(XXI)的通式(5)2-氨基-4-硬脂酰胺。 -N-(41.-甲氧基-3 1 -羧基苯基)苯胺与4 1 -(磺酰氯)-苯基偶氮-2-萘酚反应形成甲氧基化合物被甲基化为式(XVI)的染料。

著录项

  • 公开/公告号FR1581107A

    专利类型

  • 公开/公告日1969-09-12

    原文格式PDF

  • 申请/专利权人

    申请/专利号FRD1581107

  • 发明设计人

    申请日1968-07-23

  • 分类号C07C205/59;C09B1/515;C09B1/54;C09B43/00;C09B43/32;C09B45/16;G03C8/04;G03C8/08;G03C8/12;

  • 国家 FR

  • 入库时间 2022-08-23 11:56:10

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