GB841701A - 4:4-diaminodiphenylsulphoxide derivatives - Google Patents

4:4-diaminodiphenylsulphoxide derivatives

Info

Publication number
GB841701A
GB841701A GB1115557A GB1115557A GB841701A GB 841701 A GB841701 A GB 841701A GB 1115557 A GB1115557 A GB 1115557A GB 1115557 A GB1115557 A GB 1115557A GB 841701 A GB841701 A GB 841701A
Authority
GB
United Kingdom
Prior art keywords
compounds
bis
acid group
carboxylic acid
sulphoxide
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB1115557A
Inventor
George William Driver
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1115557A priority Critical patent/GB841701A/en
Publication of GB841701A publication Critical patent/GB841701A/en
Expired legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

The invention comprises compounds of the formula: <FORM:0841701/IV(b)/1> wherein R and R1 stand for hydrogen, a hydrocarbon radical having at least one sulphonic or carboxylic acid group, an acyl radical having at least one carboxylic acid group, or a glucose residue having a sulphonic acid group, provided that when R stands for hydrogen R1 does not stand for hydrogen or the b -carboxypropionyl radical, and salts of these compounds. The compounds may be used in the treatment of leprosy. Compounds in which R and/or R1 is a -sulphoethyl, a ,b -disulpho-g -phenyl-n-propyl, carboxymethyl, b -carboxypropionyl, or 1-sulphoglucosyl, are mentioned. 4,41-diaminodiphenyl-sulphoxide may be reacted with an aliphatic or aromatic saturated or unsaturated aldehyde in the presence of sulphurous acid or an alkali metal bisulphite or metabisulphite to form compounds in which R and/or R1 is a hydrocarbon radical having a sulphonic acid group. The aldehyde may be acetaldehyde, cinnamaldehyde, or glucose. To obtain a compound in which R and/or R1 is a hydrocarbon radical bearing a carboxylic acid group, 4,41-diamino-diphenylsulphoxide may be reacted with a halogeno-alkane carboxylic acid such as monochloracetic acid. Compounds in which R and/or R1 is an acyl radical bearing a carboxylic acid group may be obtained by reacting 4,41-diaminodiphenylsulphoxide with the anhydride of a dicarboxylic acid e.g. succinic anhydride. The compounds may be used in the form of their alkali metal salts e.g. the sodium and potassium salts. Examples describe the preparation of the disodium salt of 4.41-bis-glucosyl-aminodiphenylsulphoxide-a , a 1-disulphonic acid, disodium 4,41-bis-ethylaminodiphenylsulphoxide-a , a 1-disulphonate, 4-carboxymethylamino - 41 - aminodiphenylsulphoxide, disodium 4-amino-41-g -phenyl-n-propylaminodiphenylsulphoxide-a -b -disulphonate, the potassium salt of 4,41-bis-g -phenyl-n-propylaminodi-phenyl - sulphoxide - a b , a 1b 1 - tetrasulphonic acid, and 4,41-bis-(b -carboxypropionylamino)-diphenyl-sulphoxide. Di-sodium 4,41-bis-sulphinomethylamino-diphenyl sulphoxide tetrahydrate is described in the Provisional Specification.
GB1115557A 1957-04-05 1957-04-05 4:4-diaminodiphenylsulphoxide derivatives Expired GB841701A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1115557A GB841701A (en) 1957-04-05 1957-04-05 4:4-diaminodiphenylsulphoxide derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1115557A GB841701A (en) 1957-04-05 1957-04-05 4:4-diaminodiphenylsulphoxide derivatives

Publications (1)

Publication Number Publication Date
GB841701A true GB841701A (en) 1960-07-20

Family

ID=9981035

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1115557A Expired GB841701A (en) 1957-04-05 1957-04-05 4:4-diaminodiphenylsulphoxide derivatives

Country Status (1)

Country Link
GB (1) GB841701A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0083204A2 (en) * 1981-12-28 1983-07-06 Ono Pharmaceutical Co., Ltd. 2-Aminophenol derivatives and process for their preparation
EP0102476A1 (en) * 1982-08-06 1984-03-14 American Cyanamid Company Method of modulating the immune response system in mammals

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0083204A2 (en) * 1981-12-28 1983-07-06 Ono Pharmaceutical Co., Ltd. 2-Aminophenol derivatives and process for their preparation
EP0083204A3 (en) * 1981-12-28 1983-08-24 Ono Pharmaceutical Co., Ltd. 2-aminophenol derivatives and process for their preparation
EP0102476A1 (en) * 1982-08-06 1984-03-14 American Cyanamid Company Method of modulating the immune response system in mammals

Similar Documents

Publication Publication Date Title
GB799271A (en) Production of intermediates for the synthesis of reserpine and allied compounds
GB917952A (en) Production of ester type anionic surface active agents
GB935262A (en) Improved zincating compositions and baths
GB841701A (en) 4:4-diaminodiphenylsulphoxide derivatives
GB791875A (en) Process for the preparation of per-fatty acids
GB969335A (en) Cellulose and starch esters of tricarboxylic acids
GB690816A (en) Improvements in or relating to the manufacture of substituted phenoxy acetic acids
US2478978A (en) Reaction of podocarpic acid and certain halo-alkanoic acids and products thereof
GB1005472A (en) Process for the preparation of hydroxy-alkenoic acids
US2521812A (en) Ester derivatives of chloromethyl dihydrosafrol
GB515412A (en) Processes of preparing derivatives of aromatic amino-sulfamids
GB744582A (en) Improvements in and relating to the production of unsaturated acids and esters
US2724715A (en) 2-(p-carboxybenzenesulfonylamino)-5-sulfamyl-1, 3, 4-thiadiazole
GB650389A (en) Improvements in or relating to the production of salts of chloro-aryl-oxyacetic acids
Kosuge et al. Synthese of Nitoro-compounds by Means of Oxidation of Acylamino-compounds.(VI): The Catalytic Action of the Stabilizung Agents of Hydrogen Peroxid And the Mechanism of these Catalytic Action
GB924600A (en) Substituted benzyl hydrazines and semicarbazides and processes for making them
GB826360A (en) Retrocortin esters and their preparation
GB668776A (en) Chemotherapeutic agents
GB876607A (en) Alkali metal salts and alkaline earth metal salts of n-isonicotinylhydrazine n-glucuronide and a process for their production
GB727483A (en) Hydroxy derivatives of carboxylated alkylene polyamines
GB695529A (en) Process for the production of crystalline vanillyl amides
GB874362A (en) A process for the production of ª--(p-nitrobenzoyl)-ª--phthalimino acetic acid esters
GB723800A (en) Trihydroxy steroid adducts
GB435605A (en) A process for the production of condensation products from trihalogen esters of fatty acids and esters of levulinic acid
GB706661A (en) Indan compounds