Method for the hydrolysis of azetidinothiazoline compounds

This invention relates to a process for the hydrolysis of an acylthio group represented by the following reaction scheme: ##STR3## wherein R is an amino or substituted amino; Acyl is an acyl group, B is a hydroxy group or carboxy protecting group; Metal is a metal belonging to the group Ib of IIb of the periodical table; R' is ethyl, ethylene, or ethylidene group optionally substituted by alkyl or alkoxy containing 1 to 3 carbon atoms, hydroxy, alkoxyalkyl containing 2 to 5 carbon atoms, halogen, carboxylic, sulfonic, or carbonic acyloxy containing 1 to 8 carbon atoms, or amino bearing hydrogen, alkyl containing 1 to 8 carbon atoms, or alkoxyalkyl. The broken line between Rand Acyl shows the acyl carbonyl can be combined with amino R to give an azetidinothiazdine ring system.
In the above reaction scheme, the Acyl of the acylthio at position 4 can be that derived from organic acids containing 1 to 12 carbon atoms, for example, carboxylic acid (e.g. alkanoic acid, alkenoic acid, alkynoic acid, cycloalkanoic acid, aralkanoic acid, aralkenoic acid, aromatic carboxylic acid, or other carboxylic acids optionally substituted by e.g. an inert group selected from halogen, alkyl, phenyl, halophenyl, alkoxy, aryloxy, acyloxy and oxo), sulfonic acid, sulfinic acid, phosphonic acid, or other organic acids; or from inorganic acid e.g. carbonic acid, sulfuric acid, phosphoric acid, halogenic acid, hydrohalogenic acid, or other inorganic acids.
The amino substituents in the group R at position 3 can be an amino substituent constituting known side chains in the chemistry of natural or synthetic penicillins or cephalosporins, or their equivalents. The group can widely be varied, because it generally has a less direct relationship with the hydrolysis of 4-acylthio group. It can be an acyl, hydrocarbyl, hydrocarbylidene, silyl, sulfenyl, or like conventional amino substituents in the field of cephalosporin or penicillin chemistry, and containing up to 20 carbon atoms.
Representative acyl includes following groups:
(1) alkanoyl containing from 1 to 5 carbon atoms;
(2) haloalkanoyl containing from 2 to 5 carbon atoms;
(3) azidoacetyl;
(4) cyanoacetyl;
(5) acyl groups of the formula:
Ar--CQQ'--CO--
in which Q and Q' are each hydrogen or methyl; and Ar is phenyl, dihydrophenyl, or a monocyclic heterocyclic aromatic group containing from 1 to 4 hetero atoms selected from nitrogen, oxygen, and/or sulfur atoms, and may optionally be substituted by an inert group e.g. an alkyl or alkoxy group containing from 1 to 3 carbon atoms, chlorine, bromine, iodine, fluorine, trifluoromethyl, hydroxy, cyano, aminomethyl, amino, or nitro;
(6) acyl groups of the formula:
Ar--G--CQQ'--CO--
in which G is an oxygen or sulfur; and Ar, Q, and Q' are as defined above;
(7) acyl groups of the formula:
Ar--CHT--CO--
in which Ar is as defined above; and T is i) amino, ammonium, amino substituted by such conventional amino substituents as benzyloxycarbonyl, alkoxycarbonyl containing from 1 to 4 carbon atoms, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl, benzhydryloxycarbonyl, cyclopropylmethoxycarbonyl, methanesulfonylethoxycarbonyl, triphenylmethyl, 2,2,2-trichloroethoxycarbonyl, guanidylcarbamoyl, optionally substituted ureido carbonyl, alkanoyl containing from 1 to 5 carbon atoms, pyronecarbonyl, thiopyronecarbonyl, pyridonecarbonyl, homo- or heter-cyclic monocyclic aromatic acyl optionally substituted by hydroxy, lower alkanoyloxy containing from 1 to 3 carbon atoms, halogen, trifluoromethyl or alkyl containing from 1 to 3 carbon atoms, aminoalkyl containing from 1 to 3 carbon atoms, halogen, trifluoromethyl, or alkyl containing from 1 to 3 carbon atoms, or hydroxyalkyl containing from 1 to 3 carbon atoms, or amino protected in the forms of phthalimido, or of enamino derived from acetoacetates, acetylacetone, acetacetamido, or acetoacetonitrile, ii) hydroxy or acyloxy containing from 1 to 7 carbon atoms, iii) carboxy or alkoxycarbonyl containing from 2 to 7 carbon atoms, indanyloxycarbonyl, phenoxycarbonyl, or iv) azido, cyano, carbamoyl, alkoxysulfonyl, sulfo, or alkoxysulfonyl;
(8) 2-sydnon-3-alkanoyl containing from 3 to 5 carbon atoms;
(9) (2- or 4-pyridon-1-yl)acetyl;
(10) 5-aminoadipoyl, 5-aminoadipoyl protected at the amino group by aroyl or alkanoyl containing from 1 to 10 carbon atoms, chloroalkanoyl containing from 1 to 5 carbon atoms, or by alkoxycarbonyl containing from 2 to 10 carbon atoms; or 5-aminoadipoyl protected at the carboxy group by benzhydryl, 2,2,2-trichloroethyl, trialkylsilyl, alkyl containing from 1 to 6 carbon atoms, nitrobenzyl, or methoxybenzyl; and
(11) acyl groups of the formula:
L--O--CO--
in which L is an easily removable optionally substituted hydrocarbon group containing from 1 to 8 carbon atoms (e.g. 2,2,2-trichloroethyl, isobornyl, tertiary butyl, 1-methylcyclohexyl, 2-alkoxy tertiary butyl, benzyl, p-nitrobenzyl, or p-methoxybenzyl).
Alternatively, the substituent can be a diacyl group derived from a polybasic carboxylic acid containing from 4 to 12 carbon atoms, alkylidene containing from 1 to 6 carbon atoms, or arylmethylidene containing from 7 to 9 carbon atoms. In the above list of acyl groups, examples of Ar include furyl, thienyl, pyrryl, oxazolyl, isoxazolyl, oxadiazolyl, oxatriazolyl, thiazolyl, isothiazolyl, thiadiazolyl, thiatriazolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, phenyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, and dihydrophenyl, each being optionally substituted by halogen, alkyl containing from 1 to 3 carbon atoms, hydroxy, aminomethyl, or alkoxy containing from 1 to 3 carbon atoms.
Another amino substituents include a hydrocarbyl containing up to 20 carbon atoms (e.g. methyl, propyl, tertiary butyl, benzylidene, o-oxybenzylidene, trityl), silyl containing 1 to 10 carbon atoms (e.g. trialkylsilyl), sulfenyl (e.g. o-nitrophenylsulfenyl), which can, where possible, be unsaturated or substituted by an inert group e.g. halogen, alkyl, acyloxy, alkoxy or acylamino containing 1 to 8 carbon atoms, oxo, nitro and like substituents. The group convertible into amino or amido (e.g. azido, isocyanato, isocyano) is also included in the definition of the substituted amino. The silyl and sulfenyl groups are conventional protecting group for amino group. Two amino substituents on the amino can be combined to form a ring structure.
In the definition of the said 4-acylthio-3-amino-2-oxo-.alpha.-(substituted or unsubstituted)azetidine-1-acetic acid (I) is included a 3-substituted-4-thia-2,6-diaza-7-oxo-bicyclo[3,2,0]-hept-2-en-6-ylacetic acid which is a compound having combined 3-amino and 4-thio groups through an acyl.
The carboxy protecting group B can contain 1 to 20 carbon atoms, and can be an oxygen function such as, for example, alkoxy containing from 1 to 8 carbon atoms (e.g. methoxy, ethoxy, or tertiary butoxy), aralkoxy containing from 7 to 20 carbon atoms (e.g. benzyloxy, methoxybenzyloxy, nitrobenzyloxy, diphenylmethoxy, or trityloxy), mono- or bi-cyclic aryloxy (e.g. phenoxy or naphthyloxy), or organometaloxy (e.g. trimethylstannic oxy or trimethylsilyloxy), organic or inorganic acyloxy containing up to 8 carbon atoms or metal oxy of groups I, II, or III in the periodical table (e.g. sodiooxy, potassiooxy, or magnesiooxy); or B can be selected from sulfur functions such as those forming thiol ester, thiocarboxy, or like groups; nitrogen functions as these forming amides, hydrazides, azide or like groups; or B can be selected from other carboxy protecting groups.
These groups can, where possible, be interrupted by a hetero atom in their skeleton, or can be unsaturated or substituted by a substituent (e.g. the nitrogen, oxygen, sulfur, carbon, or phosphorus functions, or halogen).
Among carboxy protecting groups, are these forming haloalkyl esters containing from 1 to 5 carbon atoms, acylalkyl esters containing from 2 to 10 carbon atoms, alkoxyalkyl or aminoalkyl esters containing from 2 to 8 carbon atoms, the phenylester, aralkyl esters containing from 7 to 20 carbon atoms, ester with an oxime containing from 2 to 10 carbon atoms, N-alkoxyamide containing from 1 to 5 carbon atoms, imide with saccharin, imide with phthalimide, N,N'-diisobutylhydrazide, metal salts, alkylamine salts containing from 1 to 6 carbon atoms, or groups equivalent in effect to those groups (in the above, specified numbers of carbon atoms are for group B).
Antibacterially preferred carboxy-protecting groups B include these which from acyloxymethyl esters, phenacyl esters, the benzaldoxime ester, N,N-dimethylaminoethyl ester, methanesulfonylethyl ester, alkali metal salts, alkaline earth metal salts, acylated alkaline earth metal salts, and other groups equivalent in effect to these groups. Preferred carboxy protecting groups B include benzhydryloxy, p-nitrobenzyloxy, p-methoxybenzyloxy, 2,2,2-trichloroethoxy, and alkali metal oxy.
The process of this invention can be carried out by treating the 4-acylthio compound (I) with a salt of metal belonging to the group Ib or IIb of the periodical table to afford the 4-metalthio compound (II).
The said salt of a metal belonging to the group Ib or IIb of the periodical table can be a salt of a metal belonging to the group Ib (e.g. copper, silver) or IIb (e.g. zinc, cadmium, mercury), or their mixtures capable of cleaving the acylthio group giving the objective metal substituted thio group. The salt can be a salt of the metal with an organic acid as aliphatic acid (e.g. formic acid, acetic acid, propionic acid, succinic acid, oleic acid, lauric acid, stearic acid), aromatic carboxylic acid (e.g. benzoic acid, salicyclic acid, naphthenic acid), sulfonic acid (e.g. phenolsulfonic acid, toluene-p-sulfonic acid, trifluoromethanesulfonic acid, methanesulfonic acid), or other organic acids (e.g. citric acid, lactic acid, oxalic acid, trifluoroacetic acid); or inorganic acid as mineral acid (e.g. chloric acid, perchloric acid, bromic acid, iodic acid, periodic acid, sulfurous acid, persulfuric acid, selenic acid, nitric acid, nitrous acid, arsenic acid, phosphoric acid, pyrophosphoric acid, carbonic acid), or other inorganic acids (e.g. boric acid, sulfamic acid, carbamic acid), or double salts or complex salts (e.g. nitroprusside salts, silicofluoride, fluoroborate, a complex of mineral acid salts with alkali metal salts or ammonium salts), or their mixtures.
Among these salts, the salts highly soluble in the reaction medium, highly dissociating salts of strong acids, and the salts of silver or mercury having higher ability to capture the produced thio group, are more preferable. Specific examples of the preferable salts include AgClO.sub.4, AgIO.sub.4, AgPF.sub.6, CF.sub.3 COOAg, CF.sub.3 SO.sub.3 Ag, AgBF.sub.4, CH.sub.3 SO.sub.3 Ag, AgNO.sub.3, CH.sub.3 COOAg, Hg(ClO.sub.4).sub.2, Hg(IO.sub.4).sub.2, Hg(ClO.sub.3).sub.2, Hg(PF.sub.6).sub.2, (CF.sub.3 COO).sub.2 Hg, (CF.sub.3 SO.sub.3).sub.2 Hg, Hg(BF.sub.4).sub.2, (CH.sub.3 SO.sub.3).sub.2Hg, Hg(NO.sub.3).sub.2, (CH.sub.3 COO).sub.2 Hg, Cu(ClO.sub.4).sub.2, Zn(ClO.sub.4).sub.2, Zn(BF.sub.4).sub.2, Cd(NO.sub.3).sub.2, and ZnSiF.sub.6.
The reaction is satisfactorily effected preferably in a solvent, at room temperature or cooled or elevated temperature. The said solvent can preferably be polar organic solvent (e.g. alcohol, ketone, ether, amide, sulfoxide, nitrile, ester) or water, or their mixtures, which can contain other organic solvent, catalyzer, or radical initiator, and if required under irradiation of light, for smooth reaction. The solvent system in which the produced metalthio compounds are less soluble is preferable for simpler isolation of the product. The solvent system in which the metalthio compounds are soluble (e.g. methylene chloride, chloroform) is preferable for the chromatographic separation, or successive treatment of the next step.
The solvent for the reaction medium can be a hydrocarbon (e.g. pentane, hexane, benzene, toluene), halohydrocarbon (e.g. methylene chloride, chloroform, carbon tetrachloride, dichlorobenzene), ester (e.g. ethyl acetate, butyl acetate, methyl benzoate, butyl acetate, methyl benzoate), ketone (e.g. acetone, cyclohexanone, benzophenone), ether (e.g. diethyl ether, ethyleneglycol dimethyl ether, tetrahydrofuran, tetrahydropyrane, dioxane, morpholine, anisole), alcohol (e.g. methanol, ethanol, ethyleneglycol, benzylalcohol), carboxylic acid (e.g. acetic acid, propionic acid), base (e.g. butylamine, triethylamine, pyridine, picoline), amide (e.g. dimethylformamide, dimethylacetamide, hexamethylphosphorotriamide), nitrile (e.g. acetonitrile, benzonitrile), nitrohydrocarbon, sulfoxide, (e.g. dimethylsulfoxide), water, liquid ammonia solvents, or their mixtures.
In a reaction medium in which the product is less soluble, the reaction product separates in the medium, which can be collected by filtration, washed, and dried to give the objective compound in high yield. In a reaction medium in which the reaction product is soluble, the reaction mixture can be evaporated to remove solvents and treated with a solvent in which the product is less soluble, or be isolated by conventional methods as extraction, washing, drying, and evaporating the solvent. For the purification is used recrystallization, reprecipitation, etc.
Thus prepared 4-metal thio compound (II) can be treated with a metal removing reagent to give the 4-mercapto compound (III).
The said metal removing reagent can be a thiol compound e.g. hydrogen sulfide, or a compound capable of forming insoluble compound with the said metal (e.g. hydrochloric acid, hydrobromic acid, or their salts), or compounds capable of removing metal by forming a complex. The reaction can be carried out in a solvent given above, at room temperature, cooled or elevated temperature. The product can be isolated by conventional methods from the reaction mixture by removing unreacted material, by-products, solvents, or other impurities, and be purified by conventional methods e.g. recrystallization, chromatography, reprecipitation.
The 4-metal thio compound (II) is a novel compound useful as an intermediate for synthesizing e.g. cephalosporin compounds by cyclization, and as a medicine.
More particularly, the present invention relates to a method for preparing a compound of the formula: ##STR4## wherein R is methyl, phenyl, phenoxymethyl, or benzyl; M is Ag or Hg.sub.1/2 ; ##STR5## in which R' and R" each are alkyl or combined together form alkylene; R.sup.2 is hydroxy, methoxy, or methyl; and
R.sup.3 is methyl, ethyl, t-butyl, trichloroethyl, benzyl, methoxybenzyl, nitrobenzyl, diphenylmethyl, or trimethylsilyl;
which comprises treating a compound of the formula: ##STR6## wherein R and R.sup.1 are as defined above;
with a salt of metal selected from a group consisting of AgClO.sub.4, AgIO.sub.4, AgPF.sub.6, CF.sub.3 COOAg, CF.sub.3 SO.sub.3 Ag, AgBF.sub.4, CH.sub.3 SO.sub.3 Ag, AgNO.sub.3, CH.sub.3 COOAg, Hg(ClO.sub.4).sub.2, Hg(IO.sub.4).sub.2, Hg(ClO.sub.3).sub.2, Hg(PF.sub.6).sub.2, (CF.sub.3 COO).sub.2 Hg, (CF.sub.3 SO.sub.3).sub.2 Hg, Hg(BF.sub.4).sub.2, (CH.sub.3 SO.sub.3).sub.2 Hg, Hg(NO.sub.3).sub.2, and (CH.sub.3 COO).sub.2 Hg.
Following examples illustrate some specific embodiments of this invention. They are not intended to limit the scope thereof.

EXAMPLE 1
To a solution of methyl 4-cyclopropylmethoxycarbonylthio-3-phthalimido-2-oxo-.alpha.-isopropylideneazetidine-1-acetate (734 mg) in methanol (3 ml) is added a solution of silver perchlorate (464 mg) in methanol (3 ml), and the mixture is stirred at room temperature under argon atmosphere. After 8 hours, the separated substance is collected by filtration, and washed with ether. The crystals are dissolved in methylene chloride, filtered through a layer of silica gel, evaporated, and recrystallized from a mixture of ether and pentane. The obtained crystals (546 mg) are silver salt at the mercapto of methyl 4-mercapto-3-phthalimido-2-oxo-.alpha.-isopropylideneazetidine-1-acetate. m.p. 196.degree.-198.degree. C. Yield: 73%.
EXAMPLE 2
To a solution of methyl 4-benzoylthio-3-phthalimido-2-oxo-.alpha.-isopropenylazetidine-1-acetate (464 mg) in dioxane (8 ml) is added a solution of silver perchlorate (456 mg) in methanol (2 ml), and the mixture is stirred at room temperature under nitrogen atmosphere. After 10 hours, the reaction mixture is concentrated after addition of methanol, and the separated silver salt at the mercapto of methyl 4-mercapto-3-phthalimido-2-oxo-.alpha.-isopropenylazetidine-1-acetate is collected by filtration. m.p. 165.degree.-169.degree. C. Crop: 401 mg. Yield: 86%.
EXAMPLE 3
To a solution of methyl 4-phenylacetylthio-3-phthalimido-2-oxo-.alpha.-(1-methoxyethylidene)azetidine-1-acetate (429 mg) in acetone (3 ml) is added a solution of silver perchlorate (334 mg) in methanol (2 ml), and the mixture is stirred at room temperature under nitrogen atmosphere. After 20 hours, the reaction mixture is diluted with methanol, and concentrated. The residue is dissolved in methylene chloride, diluted with a mixture of ether and pentane to separate crystals of silver salt at the mercapto of methyl 4-mercapto-3-phthalimido-2-oxo-.alpha.-(1-methoxyethylidene)azetidine-1-acetate (189 mg), which are collected by filtration. Yield 76%.
EXAMPLE 4
In the procedure of Example 3, the said silver perchlorate is substituted with silver nitrate (265 mg) or silver acetate (260 mg) to give silver salt at the mercapto of methyl 4-mercapto-3-phthalimido-2-oxo-.alpha.-(1-methoxyethylidene)-azetidine-1-acetate.
EXAMPLE 5
To a solution of 4-acetylthio-3-acylamino-2-oxo-.alpha.-substituted azetidine-1-acetate in a solvent is added powder or solution of the silver salt, and the mixture is stirred at room temperature under nitrogen or argon as an inert gas. After the reaction, when the objective compound separated, the product is collected by filtration, washed, and dried to give the product; and when the objective compound does not separate, if required after concentration, less dissolving solvent is added to separate the objective compound.
The product is a silver salt at the mercapto of 4-mercapto-3-acylamino-2-oxo-.alpha.-substituted azetidine-1-acetate.
The reaction conditions and the physical constants of the products are listed in Tables I and II. In the table, MeOH is for methanol, Di is for dioxane, EtOH is for ethanol, DMSO is for dimethylsulfoxide, and Ph is for phenyl.
EXAMPLE 6
To a solution of 3-substituted-4-thia-2,6-diaza-7-oxo-.alpha.-substituted bicyclo[3,2,0]hept-2-en-6-ylacetate in a solvent is added silver salt, and the mixture is stirred at room temperature under nitrogen or argon as inert gas. After the reaction, when the objective compound separated, the product is collected by filtration; and when the product did not separate, if required after concentration, less dissolving solvent is added to separate the objective compound.
The product is a silver salt at the mercapto of 4-mercapto-3-acylamino-2-oxo-.alpha.-substituted azetidine-1-acetate.
The reaction conditions are listed in Table III. Abbreviations and the physical constants are identical with these of Example 5, or Table II.
EXAMPLE 7
A silver salt at 4-mercapto of 4-mercapto-3-acylamino-2-oxo-.alpha.-substituted azetidine-1-acetate is dissolved in a solvent, and to the mixture is introduced hydrogen sulfide gas at room temperature until complete precipitation. Then the reaction mixture is bubbled with nitrogen gas to purge excessive hydrogen sulfide, and filtered to remove insoluble silver sulfide. Concentration of the filtrate gives a 4-mercapto-3-acylamino-2-oxo-.alpha.-substituted azetidine-1-acetate.
The reaction conditions and the physical constants of the products are given in Tables IV and V. The abbreviations are same with these in Example 5.
EXAMPLE 8
To a solution of a silver salt at 4-mercapto of 2,2,2-trichloroethyl 4-mercapto-3-phenoxyacetamido-2-oxo-.alpha.-(1,1-dimethoxyethyl)azetidine-1-acetate (57 mg) in chloroform (5 ml) is added 10% hydrochloric acid (0.5 ml), and the mixture is stirred at room temperature for 10 minutes. After removing insoluble material by filtration, the reaction mixture is concentrated to give 2,2,2-trichloroethyl 4-mercapto-3-phenoxyacetamido-2-oxo-.alpha.-(1,1-dimethoxyethyl)azetidine-1-acetate (40 mg). Yield: 94.2%.
EXAMPLE 9
According to the methods similar to these of Examples 5 to 8, the following compounds are prepared from the corresponding 4-acetylthioazetidineacetic acid derivatives or thiadiazabicycloheptaneacetic acid derivatives:
(1) p-methoxybenzyl 4-mercapto-3-(2,2,2-trichloroethoxycarbonyl)amino-2-oxo-.alpha.-(1-hydroxyethylidene)azetidine-1-acetate;
(2) 4-mercapto-3-benzyloxycarbonylamino-2-oxo-.alpha.-isopropylideneazetidine-1-acetic acid;
(3) p-bromophenacyl 4-mercapto-3-(o-nitrophenylsulfenyl)-amino-2-oxo-.alpha.-isopropenylazetidine-1-acetate;
(4) acetoxymethyl 4-mercapto-3-(N-tertiary butoxycarbonyl-.alpha.-phenylglycyl)amino-2-oxo-.alpha.-(1-methoxyethylidene)azetidine-1-acetate;
(5) p-nitrobenzyl 4-mercapto-3-[N-tertiary butoxycarbonyl-.alpha.-(1,4-cyclohexadien-1-yl)glycyl]amino-2-oxo-.alpha.-(1-hydroxyethylidene)azetidine-1-acetate;
(6) 2,2,2-trichloroethyl 4-mercapto-3-[N-2,2,2-trichloroethoxycarbonyl)-.alpha.-(p-hydroxyphenyl)glycyl]amino-2-oxo-.alpha.-(1-methoxymethylethylidene)azetidine-1-acetate;
(7) p-bromophenacyl 4-mercapto-3-(2,2-dimethyl-4-phenyl-5-oxoimidazolidin-1-yl)-2-oxo-.alpha.-(1-hydroxyethylidene)azetidine-1-acetate;
(8) sodium 4-mercapto-3-thienylacetamido-2-oxo-.alpha.-(1-chloroethylidene)azetidine-1-acetate;
(9) p-nitrobenzyl 4-mercapto-3-tetrazolylacetamido-2-oxo-.alpha.-(1-hydroxyethylidene)azetidine-1-acetate; and
(10) .beta.-iodoethyl 4-mercapto-3-cyanoacetamido-2-oxo-.alpha.-(1-cyclopropylmethoxycarboxyethylidene)azetidine-1-acetate.
TABLE I__________________________________________________________________________ ##STR7##Re- Reac-ac- Silver tion (II)tion (I) salt Solvent time Crop YieldNo. R.sub.1 R.sub.2 R.sub.3 (mg) (mg) (ml) Temp. (hr) (mg) (%)__________________________________________________________________________ ##STR8## ##STR9## CH.sub.3 719 AgClO.sub.4 518 MeOH 6 rt 6 636 76.22 ##STR10## ##STR11## CH.sub.3 402 AgClO.sub.4 620 MeOH+Di 7+8 rt 12 388 83.13 ##STR12## ##STR13## CH.sub.3 2000 AgClO.sub.4 4000 MeOH+Di 30+30 rt 5 (1500 84)*4 ##STR14## ##STR15## CH.sub.3 100 F.sub.3 CSO.sub.3 Ag 190 MeOH+Di 2.4+0.7 rt 8 70 605 ##STR16## ##STR17## CH.sub.3 100 F.sub.3 CCOOAg 160 MeOH+ Di 2.4+0.7 rt 8 41 356 ##STR18## ##STR19## CH.sub.3 1160 AgClO.sub.4 1200 MeOH 25 rt 7 (710 68)*7 ##STR20## ##STR21## CH.sub.3 1269 429 AgClO.sub.4 1245 AgClO.sub.4 400 MeOH+Di 12+13 MeOH+Di 6+4 rt rt ON** ON** 902 (351 62 90.8)*8 ##STR22## ##STR23## CHPh.sub.2 127 AgClO.sub.4 90 MeOH 2 rt 2 (52 41.7)*9 ##STR24## ##STR25## CHPh.sub.2 112 AgClO.sub.4 160 MeOH 3 rt 4 (49 47.1)*10 ##STR26## ##STR27## CHPh.sub.2 314 AgClO.sub.4 250 MeOH 6 rt 5 (112 38.3)* 10' ##STR28## ##STR29## CHPh.sub.2 238 AgClO.sub.4 195 MeOH 4 rt 5 (87 39.3)* (R.sub.2 isomer)11 ##STR30## ##STR31## CH.sub.2 CCl.sub.3 78 AgClO.sub.4 60 MeOH 2 rt 7 54 6412 ##STR32## ##STR33## CH.sub.2 CCl.sub.3 320 AgClO.sub.4 187 MeOH 6 rt 2 180 5113 ##STR34## ##STR35## CH.sub.2 CCl.sub.3 350 AgClO.sub.4 152 MeOH 7 rt 2 175 5014 ##STR36## ##STR37## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 54.4 AgClO.sub.4 34.9 MeOH 1 rt 3 50 82.215 ##STR38## ##STR39## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 58 AgClO.sub.4 89 MeOH 1 rt 5 46 7116 ##STR40## ##STR41## CH.sub.2 CCl.sub.3 157 AgClO.sub.4 145 MeOH 1 rt 4 112 6317 ##STR42## ##STR43## CHPh.sub. 2 128 AgClO.sub.4 83 MeOH 2 rt 4 (60 50)*18 ##STR44## ##STR45## CH.sub.2 CCl.sub.3 325 AgClO.sub.4 293 MeOH 9 rt ON** 250 68.719 ##STR46## ##STR47## CH.sub.2 CCl.sub.3 195 AgClO.sub.4 130 MeOH 5 rt 15 140 65.0__________________________________________________________________________ *Yield of thiol derivative after substitution of Ag with H. **ON is for keeping standing overnight. rt: rt is for room temperature.
TABLE II__________________________________________________________________________ ##STR48##__________________________________________________________________________ NMR: .delta..sup.CDCl.sbsp. 3 (60Mc) (Numbers in paren- theses are couplingNo. R.sub.1 R.sub.2 R.sub.3 m.p.(.degree. C) IR:.nu..sub.max .sup.CHCl.sbsp.3 (cm.sup.-1 constants in__________________________________________________________________________ Hz) ##STR49## ##STR50## CH.sub.3 165-169.degree. C(d) [.alpha.].sub.D.sup .23 -248.degree. -- --2 ##STR51## ##STR52## CH.sub.3 193-198.degree. C(d) -- --3 ##STR53## ##STR54## CH.sub.3 -- -- --4 ##STR55## ##STR56## CH.sub.3 -- -- --5 ##STR57## ##STR58## CH.sub.3 194-198.degree. C(d) 1787,1777,1727, 1617. 2.53s3H,3.65s3H, 5.50d(5)1H, 5.63d(5)1H ,7.85m4H [DMSO.sub.d.s up.6 +CDCl.sub.3 (1:1)]6 ##STR59## ##STR60## CHPh.sub.2 powder -- --7 ##STR61## ##STR62## CHPh.sub.2 -- -- --8 ##STR63## ##STR64## CHPh.sub.2 -- -- --9 ##STR65## ##STR66## CH.sub.2 CCl.sub.3 powder 3420,1762,1722, 1685. 2.33s3H,3.90s3H,4.54s2 H, 4.57+4.83ABq(12)2H , 5.0-5.33m2H,6.87-7.4 3m5H, 7.77d(7)1H.10 ##STR67## ##STR68## CH.sub.2 CCl.sub.3 powder 3425,1770,1690, 1680. 2.03s3H,4.50s2H,4.84d( 2) 2H,5.03slH,5.20brs2 H, 5.36d(4)1H,5.75dd(7 ;4) 1H,6.82- 7.40m5H,7.71d (7)1H.11 ##STR69## ##STR70## CH.sub.2 CCl.sub.3 powder 3422,1775,1693, 1677,1600. 2.27s3H,4.55s2H, 4.62+4.95ABq(11)2H, 5.08-5.30mlH, 5.60-5.80mlH, 6.70-7.62m6H, 11.85slH.12 ##STR71## ##STR72## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 124-125.degree. C(d) 3410,1774,1710, 1664,1603. --13 ##STR73## ##STR74## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 103-108.degree. C 3420,1768,1737, 1686,1601,1590, 524,1497. 1.85s3H,4.65s2H, 5.32s2H,4.9-5.7m5H, 6.7-8.4m9H,8.98d (8)1H . (DMSO.sub.d.sup.6) 6) . A-6014 ##STR75## ##STR76## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 -- -- --15 ##STR77## ##STR78## CH.sub.2 CCl.sub.3 powder 3420,1788,1680, 1600. 1.57s3H,3.22s3H, 3.27s3H,4.48s3H, 4.81s2H,5.24-5.50m2H, .76-7.26m5H, 7.83d(8)1 H.16 ##STR79## ##STR80## CH.sub.2 CCl.sub.3 foam 3420,1765,1750, 1675,1650. --17 ##STR81## ##STR82## CH.sub.2 CCl.sub.3 powder 3425,1778,1710, 1664. 2.50s+2.53s3H, 4.47s2H,4.62+4.89ABq (12)2H,5.08-5.40mlH, 5.58-5.81mlH, 6.90-7.40m5H, 7.83dlH.18 ##STR83## ##STR84## CH.sub.2 CCl.sub.3 powder 3420,1775,1750, 1720,1667. --__________________________________________________________________________
TABLE III__________________________________________________________________________ ##STR85##(III) (II)Reaction Ag-salt Solvent Reaction Crop YieldNo. R R.sub.2 R.sub.3 (mg) (mg) (ml) Temp. Time(hr) (mg) (%)__________________________________________________________________________1 PhOCH.sub.2 ##STR86## CH.sub.2 CCl.sub.3 4640 AgClO.sub.4 2280 Di+H.sub. 2 O 50+10 rt 5 2950 502 PhOCH.sub.2 ##STR87## CHPh.sub.2 1000 AgClO.sub.4 830 Di+H.sub.2 O 10+25 rt 7 (755 60.3)*3 PhOCH.sub.2 ##STR88## CH.sub.2 CCl.sub.3 96 AgClO.sub.4 50 Di+H.sub.2 O 2+0.5 rt 20 80 66.24 PhOCH.sub.2 ##STR89## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 2577 AgClO.sub.4 1190 THF+H.sub.2 O+Di 25+5+10 rt 4 2198 97.85 PhOCH.sub.2 ##STR90## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 467 AgBF.sub.4 206 THF+H.sub.2 O 6+1 rt 24 565 95.46 PhCH.sub.2 ##STR91## CH.sub.2 CCl.sub.3 224 AgClO.sub.4 105 Di+H.sub.2 O 3+0.75 rt 7 258 907 PhOCH.sub.2 ##STR92## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 233 AgClO.sub.4 124 Di+H.sub.2 O 2+0.5 rt 6 218 73.sup.1)8 PhOCH.sub.2 ##STR93## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 323 AgBF.sub.4 294 THF+Di+H.sub.2 O 4+1+1.2 rt 6 210 539 PhOCH.sub.2 ##STR94## CH.sub.2 CCl.sub.3 1500 AgClO.sub.4 670 Di+H.sub.2 O 40+10 30.degree. C 5 1824 9810 PhOCH.sub.2 ##STR95## CH.sub.2 CCl.sub.3 441 AgClO.sub.4 217 Di+H.sub.2 O 9.5+2.5 rt 6 375 78.sup.2)11 PhOCH.sub.2 ##STR96## CH.sub.2 CCl.sub.3 384 AgClO.sub.4 190 Di+H.sub.2 O 8+2 rt 8 484 71__________________________________________________________________________ .sup.1) The reaction medium is irradiated with W-lamp at the begining 5 minutes of the reaction. .sup.2) The reaction is carried out in the presence of catalytic amount o azobisisobutyronitrile
TABLE IV__________________________________________________________________________ ##STR97## (IV)React- (II) Solvent Temp. Crop Yieldion No. R.sub.1 R.sub.2 R.sub.3 (mg).sup.1) (ml) (.degree. C.) (mg.) (%)__________________________________________________________________________ ##STR98## ##STR99## CH.sub.3 300 CHCl.sub.3 6 O 245 1002 ##STR100## ##STR101## CH.sub.3 224 CHCl.sub.3 6.6 O 145 843 ##STR102## ##STR103## CH.sub.3 (Ex5-3) CH.sub.2 Cl.sub.2 -- rt 1500 (84)***4 ##STR104## ##STR105## CH.sub.3 (Ex5-6) CH.sub.2 Cl.sub.2 20 rt 710 (68)***5 ##STR106## ##STR107## CH.sub.3 (Ex5-7) CHCl.sub.3 rt 351 (90.8)*** 6 ##STR108## ##STR109## CHPh.sub.2 ##STR110## CHCl.sub.3 20 CHCl.sub.3 -- rt rt 52 755 (41.7)*** (60.3)***7 ##STR111## ##STR112## CHPh.sub.2 (Ex5-9) CHCl.sub.3 -- rt 49 (47.1)***8 ##STR113## ##STR114## CHPh.sub.2 (Ex5-10) CHCl.sub.3 -- rt 112 (38.3)***9 ##STR115## ##STR116## CH.sub.2 CCl.sub.3 (Ex6-3) CH.sub.2 Cl.sub.2 rt -- --10 ##STR117## ##STR118## CH.sub.2 CCl.sub.3 330 CHCl.sub.3 20 rt 230 90.611 ##STR119## ##STR120## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 105 CH.sub.2 Cl.sub.2 6 -50 86 10012 ##STR121## ##STR122## CH.sub.2 CCl.sub.3 57 CHCL.sub.3 5 rt 40 94.213 ##STR123## ##STR124## CH.sub.2 CCl.sub.3 69 CH.sub.2 Cl.sub.2 5 rt 52 9214 ##STR125## ##STR126## CHPh.sub.2 80 CHCl.sub.3 5 rt 53 8015 ##STR127## ##STR128## CHPh.sub.2 (Ex5-17) CH.sub.2 Cl.sub.2 2 rt 60 (50)***__________________________________________________________________________ ***Overall yield from preceding reaction. .sup.1) The example No. in the parenthesies shows example number of the preceding reaction.
TABLE V__________________________________________________________________________ ##STR129##__________________________________________________________________________ NMR: .sub..delta..sup.CDCl. sbsp.3 (60Mc) (Numbers in parentheses areNo. R.sub.1 R.sub.2 R.sub.3 m.p.(.degree. C) IR:.nu. .sub.max.sup.CHCl.sbsp.3 (cm.sup.-1) coupling constants in__________________________________________________________________________ Hz) ##STR130## ##STR131## CH.sub.3 oil 1795,1750,1733 (CCl.sub.4). 1.95t(1)3H,1.96d(9.5)1H,3.3 7s3H, 4.96t(1)2H,5.04slH, 5.22dd(90.5;5)1H,5.58d(5)1H , 6.48-7.46m4H C.sub.6 D.sub.6).2 ##STR132## ##STR133## CH.sub.3 155-158.degree. [.alpha.] .sub.D.sup.23 -83.5.degree. 1792,1773,1722 (Nujol). 2.11d(10.4)1H,2.29s3H,2.34s 3H, 3.80c3H,5.47dd(10.4;5) H,5.69d(5)1H,7.85m4H.3 ##STR134## ##STR135## CH.sub.3 167.5-169.degree. 1785,1775,1725, 1668,1626. 2.10d(10)1H,2.40s3H,3.86s3H , 5.37dd(10;5)1H.5.72d(5) 1H,7.70-8.05m4H,12.3s1H.4 ##STR136## ##STR137## CH.sub.3 169-171.degree. 1790,1776,1730, 1618. 2.22d(10)1H,2.58s3H,3.78s3H , 3.94s3H,5.25dd(10;4)1H, 5.64d(4)1H.5 ##STR138## ##STR139## CH.sub.3 146-149.degree. 1791,1781,1729, 1617. 2.20d(10)1H,2.67s3H,3.88s3H , 5.59dd(10;4)1H,5.80d(4) 1H,7.9m4H.6 ##STR140## ##STR141## CHPh.sub.2 oil 3420,1770,1738, 1685. 1.89s3H,1.92d(10)1H,4.56s2H , 4.93s2H,5.08m1H,5.20-5.65 m2H,6.80-7.55m16H.7 ##STR142## ##STR143## CHPh.sub.2 foam 3420,1770,1700, 1683,1650. 1.92d(10)1H,2.22s3H,4.66s2H , 5.16-5.50m2H,6.92-7.55m 6H,12.4s1H.8 ##STR144## ##STR145## CHPh.sub.2 oil 3460,1780,1772, 1695. 1.60d(10)1H,2.53s3H,3.80s3H , 4.60s2H,5.0-5.33m2H,6.85 - 7.50m16H.9 ##STR146## ##STR147## CH.sub.2 CCl.sub.3 oil 3430,1770,1730, 1690. 2.16d(10)1H,2.36s3H,3.95s3H ,4.58s2H, 4.68dd(20;12)2H, .04-5.52m2H,6.78-7.35m6H.10 ##STR148## ##STR149## CH.sub.2 CCl.sub.3 oil 3420,1775,1758, 1674. 1.92s3H,1.99d(10)1H,3.63s2H , 4.80s1H,4.73+4.90ABq(12.5 ) 2H,5.02-5.25m5H, 6.85t(8)1H,7.34s5H.11 ##STR150## ##STR151## CH.sub.2 C.sub.6 H.sub.4 NO.sub.2 50-51.degree. 3245,1765,1740, 1668,1597,906. 191s3H,2.03d(8)1H4.51s2H,4. 80s1H, 4.99-5.10m2H,5.21s2H ,5.26- 5.54m2H,5.62-6.11m9 H.12 ##STR152## ##STR153## CH.sub.2 CCl.sub.3 oil 3430,1785,1695. 1.60s3H,2.00d(8)1H,3.27ss3H ,H,3.30s3H, 4.50s1H,4.58s2H ,4.78s2H,5.20- 5.65m2H,6.87 -7.50m5H.13 ##STR154## ##STR155## CH.sub.2 CCl.sub.3 oil 3422,1772,1692, 1678,1598. 2.13d(9)1H,2.30s3H,4.60s2H, 4.65+ 4.95ABq(11.5)2H,5.01- 5.50,m2H,6.89-7.50m6H,11.7 0s1H.14 ##STR156## ##STR157## CHPh.sub.2 foam 3440,1773,1693, 1602. 2.05d(9)1H,2.15s3H,3.92s2H, 4.59s2H,5.00-5.39m2H, 6.90-7.43m16H.15 ##STR158## ##STR159## CHPh.sub.2 foam 3415,1775,1723, 1689,1358. --__________________________________________________________________________

Method for the hydrolysis of azetidinothiazoline compounds

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

US Referenced Citations (1)

Foreign Referenced Citations (1)

Non-Patent Literature Citations (6)

Entry
Sachs, Chem. Abs. 16, 905 (1922).
Sachs et al, Chem. Abs. 20, 1605 (1926).
Klason, Chem. Ba. 20, 3407-3413 (1887).
Reid et al., "Organic Chem. of Bivalent Sulfur" vol. 1, p. 142.
Lattrell et al. II, Ann. Chem. 1937-1954 (1974).
Lattrell, Ann. Chem. 1974, 1937-1954.