GB631878A - Improvements in or relating to 1-substituted-3-cyanoguanidines and 1, 5 substituted-biguanides and method of preparing same - Google Patents

Improvements in or relating to 1-substituted-3-cyanoguanidines and 1, 5 substituted-biguanides and method of preparing same

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Publication number
GB631878A
GB631878A GB27015/46A GB2701546A GB631878A GB 631878 A GB631878 A GB 631878A GB 27015/46 A GB27015/46 A GB 27015/46A GB 2701546 A GB2701546 A GB 2701546A GB 631878 A GB631878 A GB 631878A
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GB
United Kingdom
Prior art keywords
cyanoguanidine
bis
substituted
phenylene
dodecyl
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
GB27015/46A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB631878A publication Critical patent/GB631878A/en
Expired legal-status Critical Current

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Abstract

Calcium dicyanimide is prepared by reacting calcium cyanamide with cyanogen chloride in water. Calcium hydroxide may be added. The sodium, potassium, zinc, and copper salts of dicyanimide are prepared from the calcium salt by double decomposition.ALSO:A resinous body, described as poly[methylene-bis - (1.11 - p - phenylene - 5.51 - decamethylene-biguanide)], is made by reacting 4.4-diamino-diphenylmethane with 1.11-decamethylene-bis-3.31-cyanoguanidine in presence of hydrochloric acid, water and ethanol. The hydrochloride obtained may be converted to a free base.ALSO:1 - Substituted - 3 - cyano - guanidines and 1.5-substituted biguanides are made by heating dicyanimide or a salt thereof (see Group III) with a predetermined amount of a primary or secondary amine or a salt thereof to produce a 1 - substituted - 3 - cyano - guanidine, and then, if desired, reacting the latter with a further amount of the same or a different primary or secondary amine or a salt thereof to produce a 1.5-substituted biguanide. The reaction may be in a solvent or by fusion, solvents specified being dioxane, acetone, ethanol, butanol, and ethers of ethylene and diethylene glycol. Amine salts specified are those with acetic, oxalic, benzoic, hydrochloric, sulphuric, hydrobromic, and phosphoric acids. Examples describe the preparation of the following 1 - substituted - 3 - cyano - guanidine from sodium, potassium, or calcium dicyanimide and the corresponding amine or its hydrochloride sulphate, or acetate: (1) 1-Phenyl-3-cyanoguanidine; (2) 1 - p - sulphophenyl - 3-cyanoguanidine; (3) 1 - methyl - 1 - phenyl - 3-cyanoguanidine; (4) 1-a -naphthyl-3-cyanoguanidine; (5) 1.11-p-phenylene-bis-3.31-cyanoguanidine; (6) 1-m-hydroxyphenyl-3-cyanoguanidine; (7) 1-o-hydroxyphenyl-3-cyanoguanidine; (8) 1-cyclohexyl-3-cyanoguanidine; (9) 1-butyl-3-cyanoguanidine; (10) 1-octyl-3-cyanoguanidine; (11) 1-dodecyl-3-cyanoguanidine; (12) 1-octadecyl-3-cyanoguanidine; (13) 1.1 - cylopentamethylene - 3 - cyanoguanidine; (14) 1.1 - dibutyl - 3 - cyanoguanidine; (15) 1.11 - decamethylene - bis - 3.31 - cyanoguanidine; (16) methylene-bis-(1.11-p-phenylene-3.31-cyanoguanidine); (17) 1-benzyl-3-cyanoguanidine; (18) 1-b -sulphoethyl-3-cyanoguanidine; (19) 1-isopropyl-3-cyanoguanidine; (20) 1 - p - chlorphenyl - 3 - cyanoguanidine. Further examples describe the preparation of the following from the appropriate cyanoguanidine and the appropriate amine or its hydrochloride: (21) 1.5-diphenylbiguanide; (22) 1-phenyl-5-p-sulphophenylbiguanide; (23) 1.11-diphenyl-bis - 5.51 - p - phenylenebiguanide; (24) 1-butyl-5-octylbiguanide; (25) 1-dodecyl-5-ethylbiguanide; (26) 1-butyl-5-phenylbiguanide; (27) 1 - cyclohexyl - 5 - p - sulphophenylbiguanide; (28) 1-dodecyl-5-phenylbiguanide; (29) 1 - dodecyl - 5 - p - sulphophenyl - biguanide; (30) 1-dodecyl-5-p-sulphonamidophenylbiguanide; (31) 1.1-dibutyl-5-phenylbiguanide; (32) methylene - bis - (1.11 - p - phenylene-5.51 - octylbiguanide; (33) methylene - bis-(1.11 - p - phenylene - 5.51 - phenylbiguanide); (34) poly - [methylene - bis - (1.11 - p - phenylene - 5.51 - decamethylenebiguanide)] (from 4.41-diaminediphenylmethane and 1.11-decamethylene-bis-3.31-cyanoguanidine); (35) 1-isopropyl-5-p-chlorphenylbiguanide. Amines listed as suitable for use in the process of the invention are methylamine, dimethylamine, ethylamine, b - hydroxyethylamine, diethylamine, propylamine, dipropylamine, isopropylamine, diisopropylamine, g - methoxypropylamine, butylamine, dibutylamine, hexylamine, dihexylamine, 2-ethylhexylamine, 2.2-diethylhexylamine, octylamine, dodecylamine, octadecylamine, allylamine, b -chlorallylamine, diallylamine, octadecenylamine, ethylenediamine, propylenediamine, tetramethylenediamine, hexamethylenediamine, decamethylenediamine, cyclohexylamine, dicyclohexylamine, cyclopentylamine, benzylamine, dibenzylamine, b -phenylethylamine, naphthylmethylamine, aniline, a -naphthylamine, b -naphthylamine, o-aminodiphenyl, sulphanilic acid, sulphanilamide, 2 - sulphanilamidopyrimidine, sulphanilylguanidine, 2-sulphanilamidopyrazine, 2 - sulphanilamidopyridine, 2 - sulphanilamidothiazole, aminonaphthalenesulphonic acids, aminotoluenesulphonic acids, aminophenols, aminonaphthols, toluidines, xylidines, aminoethylbenzenes, phenylenediamines, naphthylenediamines, aminobenzoic acids, ethyl aminobenzoates, aminosalicylic acids, aminobenzamides, N-ethylaniline, N1-methylaniline, chloroanilines, bromoanilines, fluoroanilines, nitroanilines, anisidines, diaminophenols, diaminonaphthols, diaminodiphenylmethanes, piperidine, 3-aminopyridine, morpholine, thiomorpholine, pyrrolidine, piperazine, and furfurylamine.
GB27015/46A 1945-09-11 1946-09-09 Improvements in or relating to 1-substituted-3-cyanoguanidines and 1, 5 substituted-biguanides and method of preparing same Expired GB631878A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US631878XA 1945-09-11 1945-09-11

Publications (1)

Publication Number Publication Date
GB631878A true GB631878A (en) 1949-11-11

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ID=22047535

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Application Number Title Priority Date Filing Date
GB27015/46A Expired GB631878A (en) 1945-09-11 1946-09-09 Improvements in or relating to 1-substituted-3-cyanoguanidines and 1, 5 substituted-biguanides and method of preparing same

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GB (1) GB631878A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3111514A (en) * 1961-02-28 1963-11-19 Lakeside Lab Inc Aminoalkylbiguanides

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3111514A (en) * 1961-02-28 1963-11-19 Lakeside Lab Inc Aminoalkylbiguanides

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