Aminoalkyl-substituted benzimidazolidin-2-ones

This invention relates to novel aminoalkyl-substituted heterocycles and non-toxic salts thereof, as well as to various methods of preparing these compounds.
More particularly, the present invention relates to a novel class of aminoalkyl-substituted heterocycles represented by the formula
Q--C.sub.n H.sub.2n --NH--R (I)
wherein Q is ##STR3## where R.sub.1 is hydrogen, halogen, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, trifluoromethyl or amino,
R.sub.2 is hydrogen, halogen, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms or trifluoromethyl,
R.sub.1 and R.sub.2, together with each other, are methylenedioxy or ethylenedioxy, and
A is --O--, --CH.sub.2 --CH.sub.2 --, or --NR.sub.3 -- where R.sub.3 is hydrogen or alkyl of 1 to 4 carbon atoms,
n is an integer from 2 to 6, inclusive, and
R is hydrogen, benzyl or ##STR4## where R.sub.4 is hydrogen, methyl or ethyl,
R.sub.5, R.sub.6 and R.sub.7, which may be identical to or different from each other, are each hydrogen, halogen, hydroxymethyl, trifluoromethyl, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, nitro, cyano, -CONHR.sub.3, --CONHOH, --COOR.sub.3, R.sub.8 O--, methylsulfonylmethyl or, when one or two of R.sub.5 through R.sub.7 are other than halogen or trifluoromethyl, also --NR.sub.3 R.sub.9,
where
R.sub.3 has the meanings defined above,
R.sub.8 is hydrogen, alkanoyl of 1 to 20 carbon atoms, alkyl of 1 to 4 carbon atoms or aralkyl, and
R.sub.9 is hydrogen, lower alkanoyl, methanesulfonyl, carbamoyl, dimethylsulfamoyl, or alkoxycarbonyl of 2 to 5 carbon atoms, and
R.sub.5 and R.sub.6, together with each other, are --O--CH.sub.2 --O, --O--CH.sub.2 --CH.sub.2 --O--, --CH.dbd.CH--CH.dbd.CH--, --O--CH.sub.2 --CONH--, --CH.sub.2 --CH.sub.2 --CONH-- or --O--CO--NH--,
and non-toxic, pharmacologically acceptable acid addition salts thereof.
The alkylene chain --C.sub.n H.sub.2n -- in formula I may be straight or branched, and preferred embodiments thereof are --CH.sub.2 --CH.sub.2 --, --CH.sub.2 --CH.sub.2 --CH.sub.2 --, --CH.sub.2 --C(CH.sub.3).sub.2 -- and primarily --CH.sub.2 --CH.sub.2 --C(CH.sub.3).sub.2 --, where the tertiary carbon atom is bonded to the nitrogen atom or the -NH-R moiety.
A subgenus thereunder is constituted by compounds of the formula I, wherein
Q, A and R.sub.3 have the meanings previously defined,
R.sub.1 is hydrogen, methoxy or amino,
R.sub.2 is hydrogen or methoxy,
n is an integer from 3 to 6, inclusive,
R is hydrogen or ##STR5## R.sub.5 is hydrogen, --OR.sub.8, --NHR.sub.9, hydroxymethyl, cyano, --CONHR.sub.3 or halogen.
R.sub.6 is hydrogen, hydroxyl or halogen,
R.sub.7 is hydrogen, chlorine, methyl or methoxy,
R.sub.8 is hydrogen, benzyl, methyl or alkanoyl, and
R.sub.9 is hydrogen, formyl, acetyl, methylsulfonyl, carbamoyl or dimethylsulfamoyl,
provided that, when R.sub.6 and/or R.sub.7 are halogen, R.sub.5 is other than --NHR.sub.9 ; and non-toxic, pharmacologically acceptable acid addition salts thereof.
A particularly preferred subgenus thereunder is constituted by compounds of the formula I, wherein
Q, A, R.sub.3, R.sub.4 and n have the meanings previously defined,
R.sub.1 is hydrogen, methoxy or amino,
R.sub.2 is hydrogen or methoxy,
R is hydrogen or ##STR6## R.sub.5 is hydrogen or hydroxyl, R.sub.6 is hydrogen, hydroxyl, hydroxymethyl, cyano, --CONHR.sub.3, --OR.sub.8 or chlorine,
R.sub.5 and R.sub.6, together with each other, are --CH.dbd.CH--CH .dbd.CH--, --OCH.sub.2 --CONH--, --CH.sub.2 --CH.sub.2 --CONH-- or --O--CONH--,
R.sub.7 is hydrogen, methyl, methoxy, hydroxyl or chlorine, and
R.sub.8 is hydrogen, benzyl or lower alkanoyl,
and non-toxic, pharmacologically acceptable acid addition salts thereof.
The compounds embraced by formula I may be prepared by the following methods, all of which involve known organic synthesis principles:
Method A
For the preparation of a compound of the formula I wherein R is a grouping of the formula III, by reacting an amine of the formula
Q--C.sub.n H.sub.2n --NH.sub.2 (IV)
wherein Q and n have the same meanings as in formula I, with a compound of the formula ##STR7## wherein R.sub.5, R.sub.6 and R.sub.7 have the same meanings as in formula I, and
R.sub.10 is hydrogen or alkyl,
under reductive amination conditions. Suitable reducing agents are complex hydrides, preferably sodium borohydride, or hydrogen in the presence of a hydrogenation catalyst, preferably platinum, palladium or nickel.
Method B
For the preparation of a compound of the formula I wherein R is a grouping of the formula III, by reducing a compound of the formula ##STR8## wherein Q, n, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 have the same meanings as in formula I, with a complex hydride, in particular sodium borohydride, or by catalytic hydrogenation with a conventional hydrogenation catalyst, for example, platinum, palladium or nickel.
Method C
For the preparation of a compound of the formula I, wherein R is a grouping of the formula III, by reacting an epoxide of the formula ##STR9## wherein R.sub.4, R.sub.5, R.sub.6 and R.sub.7 have the same meanings as in formula I, with an amine of the formula IV; or by reacting a halohydrin of the formula ##STR10## wherein R.sub.4, R.sub.5, R.sub.6 and R.sub.7 have the same meanings as in formula I, and
Hal is halogen,
with an amine of the formula IV in the presence of an acid binding agent, such as potassium carbonate, sodium carbonate or an excess of the amine IV. The halohydrin of the formula VIII converts into the corresponding epoxide VII under the reaction conditions.
Method D
For the preparation of a compound of the formula I wherein --C.sub.n H.sub.2n -- is ##STR11## where n has the same meanings as in formula I, and
R.sub.11 is hydrogen or methyl,
by reductive amination of a compound of the formula ##STR12## wherein Q and n have the same meanings as in formula I, and
R.sub.11 has the meanings defined above,
with an amine of the formula
H.sub.2 N - R (X)
wherein R has the same meanings as in formula I. Suitable reducing agents are complex hydrides, such as sodium borohydride, or hydrogen in the presence of a catalyst, such as platinum, palladium or nickel; or by reducing a compound of the formula ##STR13## wherein Q, n, R.sub.4 and R have the meanings previously defined.
Method E
For the preparation of a compound of the formula I wherein R is a grouping of the formula III, by removing the -CH.sub.2 -aryl protective group from a compound of the formula ##STR14## wherein Q, n, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 have the same meanings as in formula I, by catalytic hydrogenation with a catalyst such as platinum, palladium or nickel.
Method F
For the preparation of a compound of the formula I in which at least one of substituents R.sub.5, R.sub.6 and R.sub.7 is hydroxyl, by removing the arylmethyl protective group or groups from a corresponding compound wherein the respective hydroxyl substituent or substituents are arylmethylated. The removal of the arylmethyl group or groups is effected by catalytic hydrogenation with a catalyst such as platinum, palladium or nickel, or by ether cleavage with a hydrohalic acid or boron tribromide.
Method G
For the preparation of a compound of the formula I wherein R.sub.5 is --NH-acyl or --NH--CO--NH.sub.2, by reacting a compound of the formula ##STR15## wherein Q, n, R.sub.4, R.sub.6 and R.sub.7 have the same meanings as in formula I, and
X is an anion,
with a carboxylic acid anhydride for introduction of the acyl radical, or with a cyanate and an acid for introduction of the carbamoyl radical. At least one mol of an acid, which protects the secondary amino group by salt formation, is additionally required.
Method H
For the preparation of a compound of the formula I wherein R.sub.5 is -CONHR.sub.3, -CONHNH.sub.2 or -CONHOH, by reacting an ester of the formula ##STR16## wherein Q, n, R.sub.4, R.sub.6 and R.sub.7 have the same meanings as in formula I, and
R" is alkyl or substituted alkyl,
with a compound of the formula
NH.sub.2 --R.sub.12 (XV)
wherein R.sub.12 is hydrogen, lower alkyl, hydroxyl or amino.
Method I
For the preparation of a compound of the formula I wherein R is hydrogen or benzyl, by removing the protective group or groups from a compound of the formula ##STR17## wherein Q and n have the same meanings as in formula I,
R.sub.13 is arylmethyl, acyl or -COOR.sub.15,
R.sub.14 is hydrogen or benzyl, and
R.sub.13 and R.sub.14, together with each other, are a dicarboxylic acid radical, such as succinyl or phthalyl, or -CHR.sub.15 -,
where R.sub.15 is alkyl, arylmethyl or aryl.
When R.sub.13 is acyl or -COOR.sub.15, or R.sub.13 and R.sub.14 together are a dicarboxylic acid radical or -CHR.sub.15 -, the protective groups are removed by hydrolysis. When R.sub.13 and R.sub.14 together are a dicarboxylic acid radical, such as phthalyl, the removal may be effected by ring cleavage with hydrazine, followed by hydrolysis. When R.sub.13 and/or R.sub.14 are arylmethyl, the removal must be effected by hydrogenation in the presence of a catalyst, such as platinum, palladium or nickel. It is also possible to remove the protective group by catalytic hydrogenation when R.sub.15 in -COOR.sub.15 is arylmethyl.
Method J
For the preparation of a compound of the formula I wherein R is hydrogen, by reducing the nitro group in a compound of the formula
Q--C.sub.n H.sub.2n --NO.sub.2 (XVII)
wherein Q and n have the same meanings as in formula I, preferably by catalytic hydrogenation with conventional catalysts, such as nickel.
The starting compounds for methods A through J are either known compounds or may be prepared by known methods.
In those instances where the end products of methods A through J are racemates, these may be separated into the optical antipode components by conventional methods.
The compounds embraced by formula I are organic bases and therefore form acid addition salts with inorganic or organic acids. Examples of non-toxic, pharmacologically acceptable acid addition salts are those formed with hydrochloric acid, hydrobromic acid, sulfuric acid, maleic acid, succinic acid, formic acid, p-amino-benzoic acid, methanesulfonic acid, 8-chlorotheophylline or the like.
The following examples illustrate the present invention and will enable others skilled in the art to understand it more completely. It should be understood, however, that the invention is not limited solely to the particular examples given below.

EXAMPLE I
A mixture consisting of 5.36 gm of 3,4-dichlorophenyl-glyoxal hydrate, 4.5 gm of 1-(3-amino-n-propyl)-1,2,3,4-tetrahydro-quinoline-(2) and 200 ml of ethanol was heated at 50.degree. C. for 1 hour. Then, while cooling, it was admixed with 5 gm of sodium borohydride at 0.degree. to 5.degree. C., the mixture was stirred for 2 hours at room temperature and then acidified with hydrochloric acid, the ethanol was distilled off, and the residue was made alkaline with ammonia. 5.5 gm of the free base, m.p. 95.degree. C., of the formula ##STR18## were obtained. Its hydrochloride, m.p. 185.degree. C., was obtained by admixing the free base with the calculated amount of ethereal hydrochloric acid.
EXAMPLE 2
A mixture consisting of 11 gm of 1-(3,4-dibenzyloxyphenyl)-1-oxo-2-hydroxy-2-ethoxyethane (m.p. 114.degree. C.), 5.6 gm of 1-(3,3-dimethyl-3-amino-n-propyl)-benzimidazolinone-(2) and 225 ml of ethanol was heated for 3 hours and subsequently admixed at 0.degree. to 5.degree. C. with 8 gm of sodium borohydride. The resulting solution was allowed to stand at room temperature for 12 hours, and then acidified with hydrochloric acid and worked up as described in the preceding example. 12.7 gm of free base, m.p. 130.degree. C., of the formula ##STR19## were obtained. Its maleate, m.p. 197.degree. C., was obtained by adding a solution of maleic acid in acetonitrile to the base.
Using procedures and starting compounds analogous to those described in Examples 1 to 2, the compounds shown in the following table were also prepared. The indicated yields are in % of theory.
Table I__________________________________________________________________________Ex. Yield % M.P. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C. ##STR20## 82 1154 ##STR21## 66 maleate 1345 ##STR22## 81 maleate 2176 ##STR23## 78 1517 ##STR24## 79 succinate 948 ##STR25## 88 p-amino- benzoate 1669 ##STR26## 60 9310 ##STR27## 75 170 methane- sulfonate 18511 ##STR28## 78 amorphous12 ##STR29## 74 hydro- chloride 19413 ##STR30## 88 hydro- chloride 21514 ##STR31## 84 maleate 20915 ##STR32## 66 succinate 16816 ##STR33## 66 sulfate 25017 ##STR34## 88 13518 ##STR35## 66 12619 ##STR36## 69.5 13420 ##STR37## 72 hydro- chloride 25221 ##STR38## 87 sulfate 22522 ##STR39## 80 p-amino- benzoate 12323 ##STR40## 68 sulfate24 ##STR41## 82 hydro- chloride 21525 ##STR42## 93 9326 ##STR43## 82 sulfate 18327 ##STR44## 80 6828 ##STR45## 61 maleate 13729 ##STR46## 81 maleate 12330 ##STR47## 70 hydro- chloride 19331 ##STR48## 78 p-amino- benzoate 11832 ##STR49## 73 178 maleate 16133 ##STR50## 62 succinate 19834 ##STR51## 81 139 succinate 20635 ##STR52## 75 141 maleate 21836 ##STR53## 69 maleate 16837 ##STR54## 83 hydro- chloride 19638 ##STR55## 67 succinate 18039 ##STR56## 84 maleate 17040 ##STR57## 69 hydro- chloride 17041 ##STR58## 79 hydro- chloride 11642 ##STR59## 70 maleate 21043 ##STR60## 68 hydro- chloride 23944 ##STR61## 50 p-amino- benzoate 152,545 ##STR62## 53 p-amino- benzoate 15946 ##STR63## 38 163 hydro- chloride 14847 ##STR64## 86 hydro- chloride 18348 ##STR65## 88.5 11649 ##STR66## 95.4 12250 ##STR67## 84,5 hydro- chloride 19751 ##STR68## 86 hydro- chloride 14252 ##STR69## 83 hydro- chloride 17653 ##STR70## 77 10754 ##STR71## 64 hydro- chloride 23355 ##STR72## 75 maleate 21856 ##STR73## 70.3 hydro- chloride 19657 ##STR74## 70.3 hydro- chloride 18158 ##STR75## 62 sulfate 25959 ##STR76## 89 122 hydro- chloride 17260 ##STR77## 87 108 maleate 24261 ##STR78## 83 127 hydro- chloride 22062 ##STR79## 88 137 methane- sulfonate 17063 ##STR80## 79 183 hydro- chloride 19864 ##STR81## 68 116 sulfate 24865 ##STR82## 86 Formate 14366 ##STR83## 78 112-114 hydro- chloride . H.sub.2 O 227- 22867 ##STR84## 71 8468 ##STR85## 73 hydro- chloride 19769 ##STR86## 79 168 maleate 8870 ##STR87## 73 hydro- chloride 18771 ##STR88## 69 hydro- chloride decomp. >200.degree.72 ##STR89##73 ##STR90##74 ##STR91##75 ##STR92##76 ##STR93##77 ##STR94##78 ##STR95##79 ##STR96##80 ##STR97##81 ##STR98##82 ##STR99##83 ##STR100##__________________________________________________________________________
EXAMPLE 84
A mixture consisting of 42.5 gm of 3,4-dibenzyloxyphenyl-.omega.-bromoacetophenone, 29 gm of N-methyl-N'-(2-benzylamino-ethyl)-benzimidazolinone-(2), 25 gm of sodium carbonate and 600 ml of acetonitrile was refluxed for 2 hours. Thereafter, the precipitated inorganic products were filtered off, and the solvent was distilled out of the filtrate under a water aspirator vacuum in a rotary evaporator, the residue was taken up in 900 ml of methanol, 30 ml of an ethereal 12% hydrochloric acid solution and 15 ml of an ethereal 1% palladium chloride solution were added, and the mixture was hydrogenated in the presence of 2 gm of activated charcoal at 60.degree. C. and 6 atmospheres until 3 molar equivalents of hydrogen had been absorbed. After separation of the catalyst, about half of the methanol was distilled off, and the residual solution was admixed with 500 ml of acetonitrile. 32 gm of 1-(3,4-dihydroxyphenyl)-1-oxo-2-[(3-methyl)-benzimidazolinone-(2)-yl]-ethylaminoethane hydrochloride crystallized out which, after recrystallization from water, had a melting point of 250.degree. C. 8 gm of this aminoketone were hydrogenated in 400 ml of methanol in the presence of 1 gm of platinum oxide under standard conditions until 1 molar equivalent of hydrogen had been absorbed, and the hydrogenation product was isolated as its hydrochloride of the formula ##STR101## having a melting point of 185.degree. C. The yield was 88% of theory.
Using an analogous procedure and corresponding starting compounds, the compounds shown in the following table were also prepared:
TABLE II__________________________________________________________________________Ex. Yield % m.p. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C.85 ##STR102## 89 p-amino- benzoate 16186 ##STR103## 92 maleate 13487 ##STR104## 92 maleate 20988 ##STR105## 93 succinate 16889 ##STR106## 90 maleate 16890 ##STR107## 96 maleate 21091 ##STR108## 93 hydro- chloride 23992 ##STR109## 94 p-amino- benzoate 15993 ##STR110## 88 hydro- chloride 17094 ##STR111## 89 succinate 20495 ##STR112## 78 cycla- mate 17696 ##STR113## 93 170 methane- sulfonate 18597 ##STR114## 90 maleate 13898 ##STR115## 94 maleate H.sub.2 18099 ##STR116## 85 maleate 157100 ##STR117## 92 maleate 180101 ##STR118## 90 hydro- chloride . 2 H.sub.2 O 275102 ##STR119## 94 hydro- chloride 265103 ##STR120## 93 hydro- chloride 177104 ##STR121## 89 succinate 215105 ##STR122## 92 succinate . H.sub.2 O 128106 ##STR123## 94 p-amino- benzoate 166107 ##STR124## 91 succinate 169-71108 ##STR125## 90 p-amino- benzoate 193109 ##STR126## 84 succinate 176110 ##STR127## 90 212 p-amino- benzoate 234111 ##STR128## 92 148 p-amino- benzoate 191112 ##STR129## 90 hydro- chloride 190113 ##STR130## 89 succinate 189114 ##STR131## 90 Formiate . 1/2 CH.sub.3 CN 159115 ##STR132## 93 95 hydro- chloride 185116 ##STR133## 94 hydro- chloride 198117 ##STR134## 93 p-amino- benzoate 199118 ##STR135## 90 hydro- chloride 175119 ##STR136## 91 206 hydro- chloride 169120 ##STR137## 94 200 hydro- chloride 201121 ##STR138## 85 198 hydro- chloride 157122 ##STR139## 92 succinate 198123 ##STR140## 89 acid maleate 202124 ##STR141## 97 acid maleate 180125 ##STR142## 92 acid maleate 168126 ##STR143## 89 hydro- chloride 230127 ##STR144## 94 hydro- chloride 252128 ##STR145## 90 succinate 173129 ##STR146## 91 198 hydro- chloride 235130 ##STR147## 84 succinate 212131 ##STR148## 89 succinate 218132 ##STR149## 94 180 hydro- chloride 190133 ##STR150## 88 formate 214134 ##STR151## 92 190 hydro- chloride 225135 ##STR152## 87 hydro- chloride 170136 ##STR153## 90 193 hydro- chloride 196137 ##STR154## 96 maleate 210138 ##STR155## 96 hydro- chloride 239139 ##STR156## 93 p-amino- benzoate 152.5140 ##STR157## 90 p-amino- benzoate 159141 ##STR158## 67 163 hydro- chloride 148142 ##STR159## 81 p-amino- benzoate 190143 ##STR160## 79 hydro- chloride 262144 ##STR161## 84 maleate 202145 ##STR162## 88 maleate 202146 ##STR163## 85 180 succinate 203147 ##STR164## 88 p-amino- benzoate 196148 ##STR165## 90 180 hydro- chloride 193149 ##STR166## 72 hydro- chloride 212150 ##STR167## 69 hydro- chloride 182151 ##STR168## 76 hydro- chloride 221152 ##STR169## 82 113 hydro- chloride . H.sub.2 O 80-82153 ##STR170## 79 formate 138154 ##STR171## 72 methane- sulfonate . H.sub.2 O 120155 ##STR172## 76 hydro- chloride 252156 ##STR173## 81 sulfate 192157 ##STR174## 72 hydro- chloride 209158 ##STR175## hydro- chloride . H.sub.2 O 173-176159 ##STR176## 83 hydro- chloride amor- phous160 ##STR177## 78 156 hydro- chloride 188161 ##STR178## 86 maleate 176162 ##STR179## 62 hydro- chloride decomp. >230163 ##STR180## 57 methane- sulfonate decomp. >230164 ##STR181## 67 hydro- chloride decomp. >220165 ##STR182## 58 sulfate decomp. >240166 ##STR183## 71 hydro- chloride decomp. >230167 ##STR184## 52 hydro- chloride decomp. >230168 ##STR185## 67 hydro- chloride decomp. >220169 ##STR186## 82 methane- sulfonate decomp. >240170 ##STR187## hydro- chloride decomp. >230171 ##STR188## 61 hydro- chloride decomp. >240172 ##STR189## 69 hydro- chloride decomp.__________________________________________________________________________ >220
EXAMPLE 173
A solution of 9.1 gm of m-benzyloxy-.omega.-bromoacetophenone in 75 ml of ethanol was admixed at -5.degree. C. with 1.2 gm of sodium borohydride, and the mixture was stirred for half an hour. The resulting solution was admixed with a little hydrobromic acid, the ethanol was distilled off under reduced pressure, and the residue was taken up in ethyl acetate. The solution was extracted first with an aqueous sodium bicarbonate solution and then with water, dried and evaporated in vacuo. The residue was taken up in 45 ml of dimethylformamide, admixed with 6.57 gm of 1-(4-amino-4,4-dimethylbutyl)-benzimidazolidinone-(2) and 6.65 gm of sodium carbonate, and the mixture was stirred for 6 hours at 105.degree. C. After working up, the reaction product was isolated as its succinate of the formula ##STR190## which had a melting point of 94.degree. C. The yield was 58% of theory.
Using an analogous procedure and corresponding starting compounds, the compounds shown in the following table were also prepared:
Table III__________________________________________________________________________Ex. Yield % m.p. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C.174 ##STR191## 61 p-amino- benzoate 166175 ##STR192## 59 68176 ##STR193## 62 maleate 210177 ##STR194## 68 hydro- chloride 239178 ##STR195## 76 p-amino benzoate 152.5179 ##STR196## 73 p-amino- benzoate 159180 ##STR197## 64 122181 ##STR198## 64 sulfate 225182 ##STR199## 47 170 methane- sulfonate 185__________________________________________________________________________
EXAMPLE 183
By reacting 69.6 gm of the compound of the formula ##STR200## with 55.6 gm of chloroacetone in the presence of potassium carbonate and potassium iodide in acetone, followed by acid-catalyzed hydrolysis, 32 gm of the compound of the formula ##STR201## m.p. 182.degree. C. were obtained. A solution of 19 gm of this substance in 300 ml of methanol was admixed with 25 ml of ammonia, and the mixture was hydrogenated with Raney nickel as the catalyst at 50.degree. to 60.degree. C. and 6 atmospheres. The hydrogenation product was isolated as its hydrochloride, m.p. 267.degree.-270.degree. C., of the formula ##STR202## The yield was 15.6 gm.
EXAMPLE 184
A mixture consisting of 35 gm of 3,4-dibenzyloxy-.omega.-bromoacetophenone, 24 gm of 1-(3-benzylamino-n-propyl)-benzimidazolinone-(2), 22 gm of sodium carbonate and 300 ml of acetonitrile was refluxed for 2 hours. The reaction product of the formula ##STR203## was isolated at its bioxalate with a yield of 44 gm (m.p. 168.degree. C.). The free base (m.p. 112.degree. C.) was liberated with aqueous ammonia. 35 gm of the base were dissolved in 350 ml of ethanol, 29 ml of 2 N sodium hydroxide were added to the solution, and then a total of 6 gm of sodium borohydride were added in portions over a period of 90 minutes. The reaction product of the formula ##STR204## was isolated as the free base (m.p. 93.degree. C.).
A solution of 15 gm of the base in 150 ml of methanol was hydrogenated in the presence of 3 gm of palladized coal at 60.degree. C. and 6 atmospheres until 3 molar equivalents of hydrogen had been absorbed. After removal of the catalyst, the solution was admixed with a solution of 2 gm of succinic acid in 20 ml of hot methanol, yielding 77% of theory of the crystalline succinate, m.p. 204.degree. C., of the formula ##STR205##
Using analogous procedures and starting compounds, the compounds shown in the following table were also prepared:
Table IV__________________________________________________________________________Ex. Yield % m.p. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C.185 ##STR206## 81 170 methane- sulfonate 185186 ##STR207## 77 succinate 189187 ##STR208## 62 hydrochloride 185188 ##STR209## 91 hydrochloride 198189 ##STR210## 82 hydrochloride 182__________________________________________________________________________
EXAMPLE 190
A solution of 7 gm of the compound of the formula ##STR211## in 200 ml of methanol was hydrogenated in the presence of 1 gm of palladized coal under standard conditions until 2 molar equivalents of hydrogen had been absorbed. The hydrogenation product was isolated with a yield of 94% of theory as its maleate (m.p. 180.degree. C., with 1 mol of water of crystallization) of the formula ##STR212##
Using analogous procedures and starting compounds, the compounds shown in the following table were also prepared:
Table V__________________________________________________________________________ Yield m.p. m.p. % of ofEx. of Base SaltNo. Formula theory .degree.C. Salt .degree.C.__________________________________________________________________________191 ##STR213## 91 hydrochloride 185192 ##STR214## 92 cyclamate 176193 ##STR215## 89 maleate 134194 ##STR216## 90 succinate 204195 ##STR217## 90 hydrochloride 170196 ##STR218## 85 hydrochloride 158197 ##STR219## 86 maleate 168198 ##STR220## 91 hydrochloride 265199 ##STR221## 90 hydrochloride .times. 2 H.sub.2 275200 ##STR222## 85 maleate 180201 ##STR223## 91 maleate 157202 ##STR224## 94 maleate 138203 ##STR225## 83 succinate 176204 ##STR226## 93 p-amino- benzoate 193205 ##STR227## 92 succinate 171206 ##STR228## 93 succinate .times. H.sub.2 O 128207 ##STR229## 92 succinate 215208 ##STR230## 90 hydrochloride 177209 ##STR231## 84 formate 214210 ##STR232## 90 190 hydrochloride 225211 ##STR233## 82 hydrochloride 170212 ##STR234## 93 193 hydrochloride 196213 ##STR235## 9 hydrochloride 175214 ##STR236## 94 206 hydrochloride 169215 ##STR237## 91 200 hydrochloride 201216 ##STR238## 86 198 hydrochloride 157217 ##STR239## 84 acid maleate 202218 ##STR240## 92 acid maleate 180219 ##STR241## 92 212 p-amino- benzoate 234220 ##STR242## 93 148 p-amino- benzoate 191221 ##STR243## 92 hydrochloride 190222 ##STR244## 86 succinate 189223 ##STR245## 84 formate .times. 1/2 CH.sub.3 CN 159224 ##STR246## 89 hydrochloride 198225 ##STR247## 90 p-amino- benzoate 199226 ##STR248## 81 acid maleate 168227 ##STR249## 81 hycrochloride 230228 ##STR250## 84 hydrochloride 252229 ##STR251## 90 succinate 173230 ##STR252## 93 198 hydrochloride 235231 ##STR253## 85 succinate 212232 ##STR254## 82 succinate 218233 ##STR255## 84 180 hydrochloride 190234 ##STR256## 81 p-amino- benzoate 190235 ##STR257## 82 180 succinate 203236 ##STR258## 89 p-amino- benzoate 196237 ##STR259## 92 180 hydrochloride 193238 ##STR260## 82 hydrochloride 212239 ##STR261## 79 hydrochloride 182240 ##STR262## 79 hydrochloride 221241 ##STR263## 80 113 hydrochloride .times. H.sub.2 80- 82242 ##STR264## 75 formate 138243 ##STR265## 82 methane- sulfonate .times. H.sub.2 120244 ##STR266## 86 sulfate 192245 ##STR267## 88 173 hydrochloride 203246 ##STR268## 73.6 175 hydrochloride 216247 ##STR269## 63 hydrochloride 181248 ##STR270## 74 169 dihydro- chloride 206249 ##STR271## 72250 ##STR272## 69 hydro- chloride amor- phous251 ##STR273## 87 156 hydro- chloride 188252 ##STR274## 75 maleate 176253 ##STR275## 74 hydro- chloride decomp. >230254 ##STR276## 92 methane- sulfonate decomp. >230255 ##STR277## 88 hydro- chloride decomp. >220256 ##STR278## 87 sulfate decomp. >240257 ##STR279## 78 hydro- chloride decomp. >230258 ##STR280## 80 hydro- chloride decomp. >230259 ##STR281## 78 hydro- chloride decomp. >220260 ##STR282## 72 methane- sulfonate decomp. >240261 ##STR283## 81 hydro- chloride decomp. >230262 ##STR284## 69__________________________________________________________________________
EXAMPLE 263
A mixture consisting of 3.9 gm of the compound of the formula ##STR285## 2 gm of acetic acid anhydride and 40 ml of dimethylformamide was heated on a boiling water bath for 1 hour. Thereafter, the solvent was distilled off in vacuo, and the base was liberated with ammonia, taken up in ethyl acetate, and the solution was dried. The ethyl acetate was distilled off, and the base was admixed in acetonitrile with the calculated amount of maleic acid, yielding 3.5 gm of the maleate of the formula ##STR286## which had a melting point of 202.degree. C. after recrystallization from methanol.
EXAMPLE 264
A solution of 6.1 gm of the compound of the formula ##STR287## in a mixture of 20 ml of water and 7.5 ml of glacial acetic acid was admixed with a solution of 1.41 gm of potassium cyanate in 7.5 ml of water at 35.degree. C. After standing overnight, the base was liberated with ammonia, separated by extracting it three times with isobutanol and converted into the maleate of the formula ##STR288## were obtained. After recrystallization from water, it had a melting point of 202.degree. C.
EXAMPLE 265
A mixture consisting of 5 gm of the compound of the formula ##STR289## 100 ml of methanol and 100 ml of a concentrated aqueous ammonia solution was gently heated until a solution had formed. The solution was allowed to stand for an extended period of time, during which 4.3 gm of the base (m.p. 198.degree. C.) of the formula ##STR290## crystallized out. Its hydrochloride, obtained by acidifying an ethanolic solution of the base with hydrochloric acid, had a melting point of 235.degree. C.
Using analogous procedures and corresponding starting compounds, the compounds shown in the following table were also prepared:
__________________________________________________________________________Ex. Yield % m.p. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C.266 ##STR291## 83 172 hydrochloride 204267 ##STR292## 86 113 hydrochloride x H.sub.2 O 80-82268 ##STR293## 84 180 hydrochloride 190269 ##STR294## 84 hydrochloride 221270 ##STR295## 91 190 hydrochloride 225271 ##STR296## 86 hydrochloride 195272 ##STR297## 83.5 hydrochloride 147273 ##STR298## 77 hydrochloride 178 (decomp.)274 ##STR299## 95 hydrochloride 208 (decomp.)275 ##STR300## 90 145 hydrochloride 215 (decomp.)276 ##STR301## 88 hydrochloride 197 (decomp.)277 ##STR302## 63 157 hydro- chloride 137__________________________________________________________________________
EXAMPLE 278
69.6 gm of the compound of the formula ##STR303## and then a solution of 0.44 mol of 3-(dibenzylamino)-n-propyl chloride in 300 ml of absolute ethanol were added to a solution of 0.42 mol of sodium in 200 ml of absolute ethanol, and the mixture was refluxed for six hours. Thereafter, the precipitated sodium chloride was separated, and the liquid phase was admixed with 45 ml of concentrated sulfuric acid while stirring and cooling. After three hours 700 ml of water were added, the ethanol was distilled off, and the residual solution was made alkaline with ammonia, whereupon the compound of the formula ##STR304## precipitated out. Recrystallized from acetonitrile, the product had a melting point of 146.degree. C.
60 gm of this compound were hydrogenated in a mixture of 400 ml of methanol and 200 ml of water in the presence of 16 ml of concentrated hydrochloric acid and palladized coal at 60.degree. C. and 6 atmospheres until 1 molar equivalent of hydrogen had been absorbed. 88% of theory of the compound of the formula ##STR305## were obtained; it had a melting point of 60.degree. C.
EXAMPLE 279
A solution of 53.4 gm of the compound of the formula ##STR306## in 420 ml of methanol and 80 ml of water was hydrogenated in the presence of 20 ml of concentrated hydrochloric acid and palladized coal at 60.degree. C. and 6 atmospheres until 1 molar equivalent of hydrogen had been absorbed. 91% of theory of the hydrochloride (m.p. 315.degree. C.) of the formula ##STR307## was obtained.
EXAMPLE 280
10.1 gm of sodium hydride and 45 gm of N-(3-chloro-n-propyl)-phthalimide were added to a solution of 31.1 gm of the compound of the formula ##STR308## in 150 ml of hexamethylphosphoric triamide (hexametapol) in an atmosphere of nitrogen, and the mixture was stirred for 5 hours at 100.degree. C. The isolated raw reaction product of the formula ##STR309## was refluxed in 1 liter of ethanol with 13 gm of 85% hydrazine hydrate for 90 minutes, admixed with 21 ml of concentrated hydrochloric acid and 100 ml of water, and heated again for 20 minutes. The precipitated phthalic acid hydrazide was separated by suction filtration, and the hydrochloride (m.p. 195.degree. C. from ethanol) of the formula ##STR310## was isolated.
EXAMPLE 281
3.3 gm of sodium hydride (55%) were added to a solution of 9.2 gm of the compound of the formula ##STR311## in 40 ml of absolute hexamethylphosphoric triamide in an atmosphere of nitrogen, and after the calculated amount of hydrogen had been released, a solution of 3-benzylamino-n-propyl chloride (b.p. 140.degree. C. at 12 mm Hg) in 13 ml of hexamethylphosphoric triamide was added. The resulting mixture was stirred for 5 hours at 100.degree. C., then poured over ice, and the reaction product of the formula ##STR312## was isolated by extraction with ether and hydrolyzed without purification with 2 N hydrochloric acid, yielding 67% of theory of the hydrochloride of the formula ##STR313## which had a melting point of 152.degree.-155.degree. C.
Using analogous procedures and corresponding starting compounds, the compounds shown in the following table were also prepared:
Table VII__________________________________________________________________________Ex. Yield % m.p. of m.p. ofNo. Formula of theory Base .degree.C. Salt Salt__________________________________________________________________________ .degree.C.282 ##STR314## 84.5 175 hydrochloride x H.sub.2 280283 ##STR315## 54 hydrochloride 150284 ##STR316## 62 maleate 157285 ##STR317## 55 hydrochloride 214-216286 ##STR318## 90 hydrochloride 277-79287 ##STR319## 68 hydrochloride 237-239288 ##STR320## 75 hydrochloride 266-268289 ##STR321## 74 76 hydrochloride x H.sub.2 140.5290 ##STR322## 92 135 hydrochloride 306291 ##STR323## 89 hydrochloride 253292 ##STR324## 65 p-amino- benzoate 245293 ##STR325## 70 p-amino- benzoate 225294 ##STR326## 82 p-amino- benzoate 233295 ##STR327## 80 hydrochloride 267-70296 ##STR328## 62 maleate 179297 ##STR329## 87 81298 ##STR330## 75 hydrochloride 246299 ##STR331## 72.3 hydrochloride 185300 ##STR332## 61 hydrochloride 225301 ##STR333## 60 hydrochloride 202302 ##STR334## 89 hydrochloride 225__________________________________________________________________________
EXAMPLE 303
A solution of 174 gm of the compound of the formula ##STR335## in 700 ml of absolute hexamethylphosphoric triamide was admixed with 48 gm of sodium hydride in the form of a 55% suspension, and after the evolution of hydrogen had ceased, a solution of 341 gm of the compound of the formula ##STR336## (m.p. 76.degree. C.) in 450 ml of hexamethylphosphoric triamide was added. The mixed solution was stirred for 5 hours at 100.degree. C., then poured over ice, extracted with ether, and after evaporation of the ether from the extract the residue was dissolved in 3 liters of ethanol, and the solution was admixed with 300 ml of 5 N sulfuric acid. The next day the reaction product of the formula ##STR337## was isolated with a yield of 61% of theory (m.p. 198.degree. C.). 58.75 gm of this compound were dissolved in 1700 ml of methanol, and after addition of Raney nickel the solution was hydrogenated at 6 atmospheres and 40.degree.-60.degree. C. The compound of the formula ##STR338## was isolated with a yield of 92% of theory (m.p. 135.degree. C.). Its hydrochloride had a melting point of 306.degree. C.
The compounds of the present invention, that is, those embraced by formula I above and their non-toxic, pharmacologically acceptable acid addition salts, have useful pharmacodynamic properties. More particularly, they exhibit coronary dilating and CNS-stimulating activities in warm-blooded animals, such as rats, guinea pigs and dogs, and are therefore useful as antihypertensives, bronchospasmolytics, circulation enhancers and antidepressants.
When R in formula I is a substituent group of the formula III, the nature of the variable substituents on the phenyl moiety thereof has an effect on the predominant pharmacological activity of these compounds.
For example, when R.sub.5, R.sub.6 and R.sub.7 are lipophilic radicals or impart a lipophilic character to the substituent group of the formula III, the antidepressant activity predominates in these compounds. Such is the case, for instance, when R.sub.5, R.sub.6 and R.sub.7 are hydrogen, halogen, alkoxy, amino, alkyl or trifluoromethyl, or when R.sub.7 is hydrogen and R.sub.5 and R.sub.6 together with each other are ethylenedioxy or especially methylenedioxy.
When R.sub.5, R.sub.6 and R.sub.7 are --OR.sub.8 (where R.sub.8 is hydrogen, acyl or aralkyl), --NH--acyl, amino or hydroxymethyl, or when R.sub.5 and R.sub.6 together with each other are --O--CH.sub.2 --CONH--, --CH.sub.2 -- CH.sub.2 --CONH-- or --O--CONH-- and R.sub.7 is hydroxyl, the vasodilating activity predominates in these compounds.
Finally, when R.sub.5 is --OR.sub.8 (where R.sub.8 is hydrogen, acyl or aralkyl), R.sub.6 is --CONHR.sub.3 and R.sub.7 is especially hydrogen, the antihypertensive activity predominates in these compounds.
Illustrative of the good pharmacological activity of the compounds of the present invention are the following data, where ##STR339##
Compound B, tested for peripheral vasodilation in dogs by measurement of the blood flow through the left hind extremity after intra-arterial administration, had a 22 times longer effective half-time and was 18 times more effective than the known vasodilator isoxsuprine.
Compound A, tested for antihypertensive activity on awake, genetically hypertonic rats, produced a decrease in blood pressure of 85 mm Hg at a dosage level of 30 mgm/kg i.p.
Compound C, tested for bronchospasmolytic activity in guinea pigs, was found to have a median effective dose ED.sub.50 i.v. of 0.09 .mu.gm/kg, whereas the corresponding ED.sub.50 -value for the known, highly effective bronchospasmolytic isoproterenol is 3.0 .mu.gm/kg.
For pharmaceutical purposes the compounds according to the present invention are administered to warm-blooded animals perorally, parentereally, rectally or by the inhalation route as active ingredients in customary dosage unit compositions, that is, compositions in dosage unit form consisting essentially of an inert pharmaceutical carrier and one effective dosage unit of the active ingredient, such as tablets, coated pills, capsules, wafers, powders, solutions, suspensions, emulsions, syrups, suppositories, inhalation sprays and the like. One effective dosage unit of the compounds according to the present invention is from 0.016 to 8.33 mgm/kg body weight, preferably 0.033 to 3.3 mgm/kg body weight, depending upon the form or mode of administration and the particular compound. The higher dosages are primarily adapted for sustained release compositions.
The following examples illustrate a few pharmaceutical dosage unit compositions comprising a compound of the present invention as an active ingredient and represent the best modes contemplated of putting the invention into practical use. The parts are parts by weight unless otherwise specified.
EXAMPLE 304
Tablets
The tablet composition is compounded from the following ingredients:
______________________________________1-(3,4-Methylenedioxy-phenyl)-2-[1,1-dimethyl-3-(benzimidazolidin-2-one-1-yl)-n-propyl-amino]-ethanol maleate(see Example 55) 2 partsStearic acid 6 partsGlucose 592 partsTotal 600 parts______________________________________
Preparation
The ingredients are admixed in conventional manner, and the composition is compressed into 600 mgm-tablets. Each tablet contains 2 mgm of the active ingredient and is an oral dosage unit composition.
EXAMPLE 305
Suppositories
The suppository composition is compounded from the following ingredients:
______________________________________1-(3,4-Methylenedioxy-phenyl)-2-[1,1-dimethyl-3-(3-methylbenzimidazolidin-2-one-1-yl)-n-propyl-amino]-ethanolhydrochloride (see Example 63) 100 partsLactose, powdered 45 partsCocoa butter 1555 partsTotal 1700 parts______________________________________
Preparation
The ingredients are processed in conventional manner into 1700 mgm-suppositories, each of which contains 100 mgm of the active ingredient and is a rectal dosage unit composition.
EXAMPLE 306
Capsules
The capsule filler composition is compounded from the following ingredients:
______________________________________1-(3-Carboxymethylamido-4-hydroxyphenyl)-2-[1,1-dimethyl-3-(1,2,3,4-tetrahydro-quinol-2-one-1-yl)-n-propyl-amino]-ethanol hydrochloride (see Example 233) 200 partsLactose 440 partsCorn starch 360 partsTotal 1000 parts______________________________________
Preparation
The ingredients are intimately admixed, the mixture is milled into a powder, and 1000 mgm-portions of the powder are filled into gelatin capsules of suitable size. Each capsule is an oral dosage unit composition containing 200 mgm of the active ingredient.
Any one of the other compounds embraced by formula I or a non-toxic, pharmacologically acceptable acid addition salt thereof may be substituted for the particular active ingredient in Examples 304 through 306. Likewise, the amount of active ingredient in these illustrative examples may be varied to achieve the dosage unit range set forth above, and the amounts and nature of the inert pharmaceutical carrier ingredients may be varied to meet particular requirements.
While the present invention has been illustrated with the aid of certain specific embodiments thereof, it will be readily apparent to others skilled in the art that the invention is not limited to these particular embodiments, and that various changes and modifications may be made without departing from the spirit of the invention or the scope of the appended claims.

Number	Name	Date	Kind
3338916	Hunziker	Aug 1967
4154829	Mentrup et al.	May 1979

Number	Date	Country
631296	Nov 1961	CAX
1516714	Feb 1968	FRX
995366	Jun 1965	GBX

Aminoalkyl-substituted benzimidazolidin-2-ones

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Entry
Davoll et al., Chem. Abst., 1960, vol. 54, cols. 9896-9898.
Bottu, Chem. Abst., 1970, vol. 72, No. 111,466n.
Seki et al., Chem. Abst., 1969, vol. 71, No. 61291h.