发明名称 PROCEDIMIENTO PARA PREPARAR UN COMPUESTO UTILIZABLE, EN ES-PECIAL, PARA OBTENER ACIDOS CROMONA-2-CARBOXILICOS ENLAZADOSO UNIDOS.
摘要 <p>1,256,354. Bis-chromones. FISONS PHARMACEUTICALS Ltd. 22 April, 1969 [16 Feb., 1968], No. 7590/68. Heading C2C. Compounds of formula and their functional derivatives, are prepared by reacting a compound of formula with a compound of formula and where necessary converting the pairs of groups A 1 , As to -COCH=C(CO 2 H)-O- or a functional derivative thereof. In the formulµ, X is a carboxylic or heterocyclic ring, or an acyclic chain, which ring or chain may be interrupted by one or more heterocyclic or carbocyclic rings, by >C=O, O, S, NH, or by substituted S or NH; P, Q, T, P<SP>1</SP>, Q<SP>1</SP>, T<SP>1</SP> are each H, halogen or optionally substituted alkyl or alkoxy; L<SP>1</SP>, L<SP>2</SP> are groups capable of forming an X group; the pair of groups A<SP>1</SP>, A<SP>2</SP> is (being not necessarily identical on each ring) OM and H or COJ, H and OCD=CHOO 2 R<SP>2</SP>, OCOCOR<SP>3</SP> and H or COCH 3 , or together form the chain COCH=C(D)-O- or COCH 2 CH(D)-O-; M is H, alkali metal or C 1-6 alkyl; J is CH 3, OR<SP>2</SP>, CH 2 COD or CH = CHD; R<SP>2</SP> is H or C 1-10 alkyl, D is CO 2 R<SP>2</SP> or a group convertible thereto and R<SP>3</SP> is OH or a group convertible thereto. Details are given for the preparation of ethyl 5 - (2 - chloroethoxy)chromone - 2 - carboxylate and the iodoethoxy analogue.</p>
申请公布号 ES363708(A1) 申请公布日期 1971.01.01
申请号 ES19080003637 申请日期 1969.02.15
申请人 FISONS PHARMACEUTICAL LIMITED 发明人
分类号 C07D311/24;(IPC1-7):07D/ 主分类号 C07D311/24
代理机构 代理人
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