FR2667069A1 - New anhydrides of alditylamines and processes for their preparation - Google Patents

Abstract

New 1-amino-1-deoxy-3,6-anhydro-hexitols 1 and 1-amino-1-deoxy-2,5-anhydro-pentitols 2 of general formula (I) in which n = 1 for the compounds 1 and n = 0 for the compounds 2 and in which R is either H or COR1. Process for the preparation of the new anhydrides of alditylamines, of formula (I), characterised in that a 1-amino-1-deoxyalditol (glycamine) is reacted with at least one carboxylic acid, an anhydride or a halide of the corresponding acid in liquid hydrogen fluoride at a temperature of below about 50 DEG C, this reaction being followed if appropriate by conversion of the anhydro-glycamines obtained into corresponding amides, by means of a carboxylic acid in a manner known per se.

Description

NEW ALDITYLAMINE ANHYDRIDES
AND METHODS FOR PREPARING THEM
The present invention relates to novel alditylamine anhydrides as well as to methods for preparing them. More specifically, the invention relates to new l-amino-l-deoxy-3,6-anhydro-hexitols (3,6-anhydro-hexitylamines) and l-amino-ldeoxy-2,5-anhydro-pentitols (2, 5-anhydro-pentitylamines).

 Such compounds can find numerous applications, in particular in the field of surfactants or polymers, where the fact that their amino group can be functionalized makes them particularly advantageous, as well as in pharmacy.

 Previous literature has described related compounds, 2,5-diamino-1,4-3,6-dianhydro-mannitol and sorbitol (R. Montgomery and LF Wiggins, J. Chem. Soc. (1946), 393) and 5-amino-5 deoxy-l-4-3,6-dianhydro-4-iditol 2-nitrate (K. Klessing, SS

Chatterjee, European patent application EP 44940) which were prepared in several stages starting from 1,11-3,6-dianhydro-mannitol and sorbitol.

où n= 1 pour les composés 1 et n = O pour les composés 2 et dans laquelle le radical R est soit H soit COR1. The new l-amino-l-deoxy-3,6-anhydro-hexitols 1 and l-amino-l-deoxy-2,5-anhydro-pentitols 2, objects of the present invention, can be represented by the general formula ( I) below

where n = 1 for compounds 1 and n = O for compounds 2 and in which the radical R is either H or COR1.

 The radical R1 is constituted by a hydrogen atom or by a saturated or unsaturated, linear or branched, substituted or unsubstituted hydrocarbon radical. having for example from 1 to 20 carbon atoms, preferably from 1 to 15 carbon atoms. By way of example of such hydrocarbon radicals, mention may be made of the methyl radical. R1 can also be a cycloalkyl, polycycloalkyl or even aromatic radical.

 In patent WO 8900162 of the applicant, an improved process has been described for the preparation of 1,4-3,6-dianhydro-hexitols by dehydration of hexitols in hydrogen fluoride in the presence of a carboxylic acid, carboxylic acid anhydride or the corresponding acid halide. This process was also applied to the preparation of hexonolactones, 1,4- or 3,6-monoanhydro-hexitols, 3,6-anhydro-hexoses as well as alkyl-3,6-anhydro-hexofuranosides.

 The new compounds 1 and 2 of the present invention can be obtained as in the aforementioned patent WO 8900162, using hydrogen fluoride in the liquid state, in the presence of at least one carboxylic acid, or an anhydride or a corresponding acid halide.

 In a variant of the process which makes it possible to prepare 1-amino-1-deoxy-3,6-anhydro-hexitols 1 and 1-amino-1-deoxy-2,5anhydro-pentitols 2, it has been shown that sulfuric acid M to 10 M, at a temperature between approximately 80 and 1400C, particularly sulfuric acid approximately 6 M substantially at boiling point (1200) could nevertheless be used. The reaction yields are, however, and in all cases, lower.

 The 1-amino-1-deoxy-3,6-anhydro-hexitols 1 and the 1-amino-l-deoxy-2,5-anhydro-pentitols 2 are prepared according to the present invention by reaction of glycamine (1-amino-1 -deoxy-alditol) corresponding with at least one carboxylic acid or anhydride or a corresponding acid halide in liquid hydrogen fluoride at a temperature below about 50oC.

 The starting l-amino-l-deoxy-alditols are conveniently prepared in the literature by catalytic reduction of an aldose in the presence of hydrazine (RU Lemieux, US patent 2,830,983) or by catalytic reduction of a benzylglycamine (F. Kagan , MY

Rebenstorf and E.J. Heinzelmann, J. Am. Chem. Soc. 79 (1957) 3541).

Glycamines or their salts, hydrochlorides, hydrobromides, etc. may be used as starting materials indifferently.

 For compounds 1 and 2 in which the radical R is COR, a carboxylic acid will be reacted with the anhydro-glycamines obtained to convert them into corresponding amides in a manner known per se.

 For the sake of simplification of terminology, the term "carboxylic acid" will be used in the present description to denote both the carboxylic acid and the corresponding anhydride or halide. Likewise, the expression "carboxylic acid" may represent, where appropriate, several carboxylic acids.

 Formic acid is the most commonly used carboxylic acid because of its low cost, as well as its ease of elimination at the end of the reaction. Higher homologs can nevertheless be used, as can the anhydrides of carboxylic acids or the anhydrides of corresponding acids, but in this case the reaction is slower.

 The action of the carboxylic acid being catalytic, it is not necessary to use stoichiometric proportions with respect to the starting compound. Thus, the molar ratio of the carboxylic acid to the starting compound may be between 0.1 and 1, without it being excluded that a lower or higher ratio also gives results. It has been observed, however, that when the proportion of carboxylic acid exceeds the equimolarity threshold, this had the effect, by diluting the hydrogen fluoride, of correlatively reducing the rate of dehydration of the starting product reacted and d '' increase the time to obtain anhydrides from this product. Indeed, the optimal concentration of the starting glycamine compared to hydrogen fluoride is in a 1/4 ratio. However, it should be understood that, in practice, the concentration can vary around this optimal value.

 The reaction is generally carried out at room temperature, the temperature at which the hydrogen fluoride which dissolved the starting materials is liquid. However, a slight rise in temperature, to 400 or 50 "C, can reduce the reaction time. In this case, a closed container must be used so that the hydrogen fluoride remains in liquid form. Likewise, a temperature below ambient temperature can be chosen, for example O C.

 At the end of the reaction, the reagents are removed by entrainment by a stream of air or inert gas, an operation possibly followed by entrainment by a cosolvent. Acid residues can, when necessary, be neutralized by the action of alkaline agents or the passage of the aqueous solution over ion exchange resin.

 A preferred implementation of the process of the invention is described below. In a polyethylene or steel container, glycamine is added with approximately four parts of hydrogen fluoride and in an equimolecular proportion with respect to glycamine, a carboxylic acid, its anhydride, or l corresponding acid halide. The reaction mixture is then maintained at a temperature close to ambient for periods of the order of 24 h. After elimination of the reagents, or the anhydro-glycamines 1, 2 are obtained in amorphous form and most often recrystallized from a suitable solvent.

The examples which are given will relate to the preparation of 1-amino-1-deoxy-3, 6-anhydro-D-glycitol 3, 1-amino-1-deoxy-3, 6-anhydro-D-mannitol 4 and 1- amino-1-deoxy-2,5-anhydro-D-xylitol 5 since the corresponding glycamine precursors are the most accessible. It goes without saying, however, that the process applies to all hexitylamine and pentitylamine. The 3-5 anhydro-glycitylamines can then be conveniently converted to the corresponding amides by the action of carboxylic acids according to known methods, or also stored in the form of salts, as described in the Examples.

 The following Examples illustrate the invention without limiting it.

 Example 1: Preparation of 1-amino-1-deoxy-3,6-anhydro-D glucitol fluorhydrate.

 The 1-amino-1-deoxy-D-glucitol (1 g) is dissolved in hydrogen fluoride (5 ml) and added with formic acid (0.2 ml). The solution is kept at 20 ° C. for 24 h then concentrated by passing an air stream or else under reduced pressure leading to an oil (1.2 g, substantially quantitative yield) characterized in the form of its tri-O derivative -acetyl-1-deoxy-1-phthalimido obtained by successive action of phthalic anhydride and acetic anhydride in pyridine pf 145-146 "C, [a] D + 310 (c 0.1, chloroform).

 Example 2: Preparation of 1-amino-1-deoxy-3, 6-anhydro-D-mannitol.

a) In hydrogen fluoride
The 1-amino-1-deoxy-o-mannitol (1.2 g) in hydrogen fluoride (5 ml) is added with formic acid (0.2 ml) and the solution is kept at room temperature for 24 h then concentrated under reduced pressure. The residue is redissolved twice in methanol and the solution is concentrated. The residue, consisting of 1-amino-1-deoxy-3,6-anhydro-D-mannitol hydrofluoride, crystallizes from ethanol (880 mg, 80%), pf

 166-168 C, [α] D-8.5 (c 1.2, water).

b) In sulfuric acid
The 1-amino-1-deoxy-D-mannitol (1.5 g) is dissolved in 6 M sulfuric acid (5 ml) and the solution is brought to reflux for 4 days. The reaction mixture is then neutralized by passage over a column of Amberlite IRA-400 resin (OH, 20 ml) then the solution is acidified by addition of hydrochloric acid.

The solution is concentrated under reduced pressure and the residue, consisting of 1-amino-1-deoxy-3, 6-anhydro-o-mannito1 in hydrochloride form, crystallizes from ethanol (690 mg, 50%), m.p.

 165-167 C, [a] D-8.5 (c 0.09, water).

 Example 3: Preparation of 1-amino-1-deoxy-2,5-anhydro-D-xylitol fluorhydrate.

 1-amino-1-deoxy-D-xylitol hydrobromide (1.5 g) is supplemented with hydrogen fluoride (4 ml) and formic acid (0.2 ml) and the solution is kept at room temperature for 24 h, then concentrated by passing an air stream or under reduced pressure. The residue is then coevaporated with methanol (10 ml) twice and recrystallized from hot water (0.5 ml) by addition of ethanol (10 ml) (530 mg, 81%), m.p. 179-181 C, [α] D +0.8 (c 0.01, water).

Claims (9)

 1. New alditylamine anhydrides of general formula (I) below

 in which n is an integer equal to O or 1 and R is chosen from H and the radicals of formula COR1, where R1 is either H or a hydrocarbon radical R2.  2. New 1-amino-1-deoxy-3,6-anhydro-hexitols according to claim 1, characterized in that the integer n of formula (I) is equal to 1.  3. New 1-amino-1-deoxy-2,5-anhydro-pentitols according to claim 1 characterized in that the integer n of formula (I) is equal to 0.  4. Compounds according to any one of claims 1 to 3 in which said hydrocarbon radical R2 has from i to 20 carbon atoms, in particular from 1 to 15 carbon atoms, and is chosen from the alkyl, cycloalkyl, polycycloalkyl and aryle.  5. Compounds according to claim 4, in which said hydrocarbon radical R2 is the methyl radical.  6. Process for the preparation of alityitylamine anhydrides according to any one of claims 1 to 5, in which a l-amino-l-deoxy-alditol (glycamine) is reacted with at least one carboxylic acid, an anhydride or a corresponding acid halide in liquid hydrogen fluoride at a temperature below about 50 C, this reaction being optionally followed by a transformation of the anhydro-glycamines obtained into corresponding amides by means of a carboxylic acid, a way known per se.  7. The method of claim 6 wherein said starting carboxylic acid is formic acid.  8. Method according to any one of claims 6 and 7 wherein the molar ratio of said carboxylic acid or anhydride or acid halide relative to the starting glycamine is between 0.1 and 1.  9. A process for the preparation of alditylamines according to any one of claims 1-5 in which a l-amino-l-deoxy-alditol is reacted in sulfuric acid from about M to about 10 M, at a temperature d 'about 80 to 140 C and the reaction mixture formed at the end of the reaction is neutralized.