CN1055736A - 4, the preparation method of 4-dialkyl group-2-azetidinones - Google Patents
4, the preparation method of 4-dialkyl group-2-azetidinones Download PDFInfo
- Publication number
- CN1055736A CN1055736A CN91103499A CN91103499A CN1055736A CN 1055736 A CN1055736 A CN 1055736A CN 91103499 A CN91103499 A CN 91103499A CN 91103499 A CN91103499 A CN 91103499A CN 1055736 A CN1055736 A CN 1055736A
- Authority
- CN
- China
- Prior art keywords
- amino
- compound
- milliliters
- tertbutyloxycarbonyl
- dimethyl
- 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.)
- Withdrawn
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
Abstract
Disclose a kind of method of preparation formula IV compound, comprised that the complex compound with formula V makes the sulfonation of formula II compound, the compound with the alkaline purification gained makes it cyclisation then.Each group definition is seen specification sheets in the formula.
Description
June 29 nineteen eighty-two, the United States Patent (USP) of issue was described the O-sulfation beta-lactam hydroxamic acid with anti-microbial activity for 4,337, No. 197, and the preferred compound of this patent disclosure has following structural formula:
Wherein, R
1', be acyl group, R
3' with R
4' identical or different, respectively be hydrogen or alkyl, M
Be hydrogen or a positive ion.
Introduce the several methods of preparation above-claimed cpd, had the intermediates preparation of following structural formula comprising a kind of utilization.
Wherein, A ' is the protecting group of a nitrogen, and Y ' is phenmethyl or pivalyl.This patent points out that the hydroxyl of above-mentioned intermediate can utilize, for example a kind of classical reagent (as methylsulfonyl chloride) is converted into leavings group.The compound that this quilt adequately protects has following structural formula (L ' be a leavings group):
This compound can be handled and cyclisation through alkali (as salt of wormwood), generates the compound with following structural formula.
This patent is given an account of the another kind of step cyclization method that continues, comprising handling the intermediate with following structural formula with triphenyl phosphine and diethylazodicarboxylate.
Have now found that (3 sulphur (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-and 2-oxo ethylidene) amino) the oxygen base) acetate is a kind of medicinal excellent antibacterial agent that is suitable for, its structural formula is as follows:
Be preparation (3 sulphur (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-and 2-oxo ethylidene) amino) the oxygen base) acetate, require to improve United States Patent (USP) 4,337,197 methods of being introduced.
Have now found that to have following structure formula II
But compound sulphur
Compound.The compound of general formula III is the intermediate of a class novelty, and is just constituting integral part of the present invention with this role.The cyclisation of abundant protected general formula III compound generates useful as intermediates, and it has following structure formula IV
Used symbol definition is as follows in general formula II, III and IV and whole specification sheets:
A is benzyloxycarbonyl, right-the nitro benzyloxycarbonyl, tert-butoxycarbonyl, neighbour-oil of mirbane sulfinyl or trityl;
R
1, R
2It for identical or different carbonatoms 1 to 4 alkyl;
R
3Be benzyl, right-nitrobenzyl, benzyloxymethyl, 2-methoxyl group-2-propyl group, 2-oxyethyl group-2-propyl group, tetrahydropyrans-2-base, 2-trimethyl silyl ethyl, t-butyldimethylsilyl or t-butyldiphenylsilyl;
The salt that is suitable for medicinal generalformula comprises by formula I compound and subsalt organic and that inorganic cation forms.They are ammonium salt, an alkali metal salt (as sodium salt, sylvite), alkaline earth salt (as calcium salt, magnesium salts) and from organic bases, for example dicyclo hexylamine, N, N '-dibenzyl-ethylenediamin, N, N '-two (dehydroabietic acid base) quadrol, N-methyl D-glycosamine deutero-salt.
The compound diagram of formula I, VI and IX is done acid, but they also can be used as zwitter-ion (inner salt) existence, and these are also included within " being suitable for medicinal salt " definition, all belong to category of the present invention.
Be suitable for medicinal (3 sulphur (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene)-amino) the oxygen base) acetate compares with other O-sulfation beta-lactam hydroxamic acid, it is unexpected excellent antibacterial agent, more clearly say, salt of the present invention, having can be by the good characteristic of Mammals oral absorption, combine with its good stability, have reliable stability clinically beta-lactam to β-Nei Xiananmei; It also has good chemical stability.
The salt that is suitable for medicinal generalformula can be used for treating Mammals, for example domestic animal (as dog, cat, horse and other Mammalss) and human gram-negative bacteria infect, this salt is particularly suitable for oral, and in the past penicillin and cephalosporin all modes of being applied in infection site also can adopt.
When the gram-negative bacteria in the treatment mammalian organism infects, be suitable for the dosage of the salt of medicinal generalformula, be about 1 milligram/kg body weight/sky to 350 milligrams/kg body weight/sky, optimum quantity is about 10 milligrams/kg body weight/sky to 100 milligrams/kg body weight/sky.
The salt that is suitable for medicinal generalformula is used for can be made into tablet, capsule, solution or aqeous suspension when oral.
In compound with following structure formula II:
Because of it is the trimethyl carbinol,, hydroxyl wherein becomes complicated so being converted into easy leavings group.Have found that, if a general formula II compound apparatus has following structural formula (V)
A kind of pyridine (or homologue of pyridine)-sulphur trioxide complex compound sulfonation (wherein: m is 0,1,2 or 3), reaction will obtain having the compound of following structure formula III with high yield,
Preferential and the hydroxyl reaction (desirable just) of pyridine-sulphur trioxide complex compound:
Sulfonation reaction can be carried out in organic solvent, and these solvents are as pyridine, and one, two or trimethylpyridine, chlorinated hydrocarbon (as methylene dichloride, 1, the 2-ethylene dichloride), acetonitrile, dimethyl formamide be with diox.The reaction optimum temps is about 0～100 ℃.
With alkali is media, the compound cyclisation of general formula III can be generated corresponding intermediates, and its structural formula is as follows:
Alkali is mineral alkali preferably, for example alkaline carbonate (resembling yellow soda ash or salt of wormwood) and should be excessive (be about general formula III reactant 2～10 times), react in the mixture that is preferably in a kind of aqueous organic solvent and carry out, organic constituent can be ethyl acetate, acetonitrile, acetone, ethyl methyl ketone, methyl propyl ketone, propyl acetone, methyl, isobutyl ketone, 1,2-ethylene dichloride, pyridine or, two or trimethylpyridine,
A kind of intermediate of general formula IV can be used to prepare a kind of antiseptic-germicide, this medicine is the salt with compound of following structural formula.
As United States Patent (USP) 4,337, described in 197, the protecting group " R on the general formula IV intermediate
3" can at first be removed, generating corresponding hydroxamic acid, its structural formula is as follows:
Remove various " R
3" reaction of group, well-known in the present technique field, certainly, this will depend on " R
3" characteristics of group itself.
The compound of general formula VII can generate the corresponding compounds with following structural formula through sulfonation:
Or their subsalt, above process can be finished by general formula VII compound and a kind of sulphur trioxide-pyridine (or dimethyl formamide, 2,6-lutidine) complex compound reaction.
3-amino protecting group " A " is removed from the compound of general formula VIII, and the result generates corresponding key intermediate, and its structural formula is as follows:
Remove the characteristics that step that protecting group takes will depend on protecting group itself.
With regard to preparing required formula I product, with R in the general formula IX
1And R
2Be methyl) a kind of compound, that is:
With a kind of carboxylic acid cpd acidylate, the carboxylic acid cpd structural formula is as follows:
Wherein, R is a carboxylic acid protecting group, promptly removes with well-established law subsequently.Above-mentioned acylation is common, just can finish with carboxylic acids such as halogenated carboxylic acid, carboxylic acid anhydride or active ester.
Further specify method of the present invention below for example, this method is used for preparation (3S(Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-and 2-oxo ethylidene) amino) the oxygen base) acetate, as the component of a kind of chiral raw material and a kind of racemic mixture.
Example 1
(3 ± (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene) amino) oxygen base) acetate disodium salt.
A) N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-D, L-3-hydroxyl valine amide
With 24.84 gram (106.6 mmole) N-tertbutyloxycarbonyl-D, the solution that L-3-hydroxyvaline and 16.33 gram (106.6 mmole) hydroxybenzotriazole-hydrates are dissolved in 500 milliliters of anhydrous tetrahydro furans is chilled to-10 ℃ of addings 22 gram (106.6 mmole) dicyclohexyl carbodiimides.Mixture stirred 1 hour in 0 ℃ under the nitrogen protection.Then, in 15 minutes, will be dissolved in the gram of 13.13 in 250 milliliters of anhydrous tetrahydro furans (106.6 mmole) O-benzylhydroxylamine solution, add in the above-mentioned ester mixture that has been activated.The mixture that generates under the nitrogen protection, was stirred 1 hour in 0 ℃.The filtering insoluble substance, with filtrate in a vacuum stripping be spumescence, the foam ethyl acetate extraction, the material of filtering indissoluble again, filtrate is with 5% sodium hydrogen carbonate solution washed twice.Organic phase drying (using sodium sulfate), flash to pulpous state, use 130 milliliters of isopropyl ethers again, obtain 24.7 gram title compounds, fusing point: 76-78 ℃ its crystallization.Mother liquid evaporation pulp (10 gram), again it is carried out chromatographic separation (this stationary phase is seated in the trichloromethane) with a pillar that includes 300 gram silica gel formulation C C-4, at first use 1 liter of this post of trichloromethane wash-out, then with 2 liters of trichloromethane wash-outs that contain 2% methyl alcohol.Back a kind of solvent elution addition product (thin-layer chromatography Rf:0.9, trichloromethane/methyl alcohol, 3: 1) and move to the impurity of solvent front.The cut of collecting flashes to soup compound (8 gram) in a vacuum, obtains 5 with 25 milliliters of isopropyl ethers after with its crystallization and restrains another kind of title compound, fusing point: 76-78 ℃.
B) N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-D, L-3-(sulphur oxygen base) the valine amide pyridinium salt.
Anhydrous pyridine (8.08 milliliters, 0.10 mmole) is contained in-500 milliliters the round-bottomed flask; and under the nitrogen protection, be chilled to-10 ℃; drip (in intense electromagnetic stirs) chlorsulfonic acid trimethylammonium first estersil (15.6 milliliters, 0.10 mmole) again; after adding; very thick reactant (because product precipitation) is stirred half an hour in 0 ℃; extract trimethylchlorosilane in a vacuum, obtain 15 gram pyridine-sulphur trioxide complex compounds.
With the N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-D, L-3-hydroxyl valine amide (16.92 grams, 50 mmoles) is dissolved in 200 milliliters of anhydrous pyridines, adds 9.87 gram (62.5 mmole) pyridine-sulphur trioxide complex compounds again.Mixture in 55 ℃ of stirrings 2 hours, adds another part (790 milligrams, 5 mmoles) pyridine-sulphur trioxide complex compound again under the nitrogen protection, continue to stir 1 hour.Thin-layer chromatography (it is a kind of that propyl carbinol/acetic acid/water (3: 1: 1) shows that product only has, and the Rf:0.77(raw material has moved to the solvent front).Reaction mixture is stripping in a vacuum, a kind of oil, this oil is used the acetonitrile stripping three times in a vacuum, rough foamed title compound, output is considered to quantitative property.
C) (3 ±)-3-((tertbutyloxycarbonyl) amino)-4,4-dimethyl-1-(benzyloxy)-the 2-azetidinone.
To fill thick N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-D, L-3-(sulphur oxygen base)-flask of valine amide, pyridinium salt (about 50 mmoles) puts into ice bath and adds 400 milliliters of ethyl acetate, add 90 milliliters of wet chemicals (containing 42.8 grams, 0.31 mole of salt of wormwood) again with violent stirring.The mixture that generates is under the nitrogen protection, through violent stirring backflow (oil bath, 95 ℃ of temperature) 2 hours.Reaction mixture is chilled to room temperature and is separated, and water is with 2 * 200 milliliters of ethyl acetate extractions, and all organic phases are returned together, and dry (use sodium sulfate) also evaporates in a vacuum.This oil is poured in 125 milliliters of 40% ethyl acetate/normal hexane mixed solvent, and with 3～4 liters of 40% ethyl acetate/normal hexane solvent above-mentioned solution is filtered rapidly by the filtering layer (10 cm thick) of-350 milliliters of SilicARCC-7 types (silica gel).Filtrate is evaporated in a vacuum, obtains a kind of solid (12.2 gram), with its crystallization in 50 milliliters of isopropyl ethers, obtains 7.15 gram title compounds, and its fusing point is 110 ℃.Mother liquid evaporation get 4.75 the gram gummy solids, contain approximately 15% by product (according to
1The H nuclear magnetic resonance spectrum).
D) (3 ±)-3-((tertbutyloxycarbonyl) amino)-1-hydroxyl-4,4-dimethyl-2-azetidinone
Under normal pressure and room temperature, with (3 ±)-3-((tertbutyloxycarbonyl) amino)-4,4-dimethyl-1-(benzyloxy)-2-azetidinone (8.07 grams, 25 mmoles) puts into 40 ml methanol, with 0.6 10% palladium that restrains, loads on the gac is catalyzer, hydrogenation 2 hours.Reaction mixture filters by the celite filtering layer, and filtrate concentrates in a vacuum.Add acetonitrile revaporization in the above-mentioned enriched material, repeat twice.Obtain 5.78 gram solid foam shape title compounds.
E) (3 ±)-3-((tertbutyloxycarbonyl) amino)-2-oxygen base-4,4-dimethyl-1-azelidinyl sulfuric acid, sylvite
Under the protection of argon and 0 ℃; pyridine-sulphur trioxide complex compound (8.02 grams, 50 mmoles) is added in the following solution in batches; this solution is by (3 ±)-3-((tertbutyloxycarbonyl) amino)-1-hydroxyl-4, and 4-dimethyl-2-azetidinone (5.78 grams, 25 mmoles) is dissolved in anhydrous pyridine (120 milliliters) and makes.Reaction mixture at room temperature stirred 2.5 hours and concentrated in a vacuum, residue is dissolved in 32 milliliters by 10% acetone: in water-based buffering (PH7) solution that the 0.5M potassium primary phosphate is formed, potassium hydroxide with 1N transfers to 5.2 with pH value, and this material is with 270 milliliters of Dowex-50(K
+) resin is by 10% aqueous acetone solution drip washing, carries out chromatographic separation.Merge the cut that is fit to and also concentrate in a vacuum, obtain the thick product of 13.6 grams.It is further refining with chromatography, operating process is: thick product is passed through 680 milliliters of HP-20 resins, earlier with 200 ml water drip washing, use 10% aqueous acetone solution drip washing again, compile suitable cut, freeze-drying (lyophilization in a vacuum) obtains 7.13 gram title compounds, and its fusing point is 163～170 ℃ of decomposition.
F) (3 ±)-3-amino-2-oxygen base-4,4-dimethyl-1-azelidinyl vitriol
Under the protection of argon and-10 ℃, with (3 ±)-3-((tertbutyloxycarbonyl) amino)-4,4-dimethyl-1-azelidinyl sulfuric acid sylvite (5.48 restrain, 15 mmoles) in-10 ℃ of low suspensions in 20 milliliters of anhydrous methylene chlorides.Add methyl-phenoxide (6 milliliters), add 26 milliliters of trifluoroacetic acids with clock more than 2 minutes immediately.Reaction mixture stirred 20 minutes down in-10 ℃, concentrated in a vacuum then, and residue is with ether (three times) porphyrize, and is dry in a vacuum, obtains rough white solid title compound.
G) (3 ± (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene) amino) oxygen base) acetate, phenylbenzene methyl esters, sodium salt
With (Z)-(2-amino-4-thiazolyl) (((2-phenylbenzene methoxy base)-2-oxo oxyethyl group) imido grpup) acetate (6.52 gram, 16 mmoles) and triethylamine (2.5 milliliters, 18 mmoles) under-30 ℃, argon protection, same being dissolved in 60 milliliters of dimethyl formamides.Drip diphenyl phosphate chloride (3.5 milliliters, 17 mmoles), reaction mixture stirred 1.5 hours down at-30 ℃.
With thick (3 ±)-3-amino-2-oxygen base-4 of above preparation, 4-dimethyl-1-azelidinyl vitriol is dissolved in 10 milliliters of dimethyl formamides in 0 ℃, and adds 6.6 milliliters of triethylamines.In the mixed anhydride with this drips of solution superimposed under-30 ℃.Reaction mixture stirred 3.5 hours down at-30～-20 ℃, rose to room temperature again.With the insolubles filtering, filtrate concentrates in a vacuum.Residue is dissolved in 60 milliliters, and by 20% acetone: in the damping fluid that the 0.5M SODIUM PHOSPHATE, MONOBASIC is formed (PH7), the sodium hydroxide solution with 2N transfers to 6.0 with PH again.With 300 milliliters of DoWex-50(Na
+) resin is stationary phase, 20% aqueous acetone solution is that moving phase is refining with this solution chromatographic separation.Compile suitable cut, freeze-drying.Crude product is dissolved in 200 milliliters contains in the water-acetonitrile, the insoluble inorganic salt of filtering.Filtrate concentrates in a vacuum, obtains 19.32 gram title compounds (containing raw material acid impurity).
H) (3 ± (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl)-amino)-2-oxo ethylidene) amino) oxygen base) acetate, disodium salt.
With rough (3 ± (Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2; 2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl)-amino)-2-oxo ethylidene) amino) the oxygen base) acetate, phenylbenzene methyl esters, sodium salt (19.3 gram) at-10 ℃, argon protection low suspension in 50 milliliters of methylene dichloride and 6 milliliters of methyl-phenoxide mixed solvents; add trifluoroacetic acid (90 milliliters); reaction mixture was stirred 1 hour; concentrate in a vacuum, with ether (three times) porphyrize.This crude product is dissolved in the phosphate sodium dihydrogen buffer solution of 40 milliliters of 0.5M (PH is 7), the sodium hydroxide solution with 2N transfers to 6.8 with PH again.This solution is that stationary phase, water are that moving phase is carried out chromatographic separation with 900 milliliters of HP-20.The cut that is suitable for is divided into two portions, and not too pure part is carried out chromatographic separation with 500 milliliters of HP-20 again.The suitable cut that compiles twice chromatographic separation gained, freeze-drying obtain 3.8 gram title compounds, its fusing point: be 195～210 ℃ of decomposition.
To C
12H
13N
6O
9S
2Na
224H
2O analyzes and calculates:
C，27.46;H，3.41;N，13.35;S，12.22
Measure:
C，27.46;H，3.48;N，13.06;S，12.04
Example 2
(3S(Z))-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene) amino) oxygen base) acetate, disodium salt
A) N-(tertbutyloxycarbonyl)-L-3-hydroxyvaline α-methylbenzyl amine salt
N-tertbutyloxycarbonyl-beta-hydroxy Xie Ansuan (7.02 gram, 30 mmoles) is dissolved in solution that 250 milliliters of ether make with 3.63 gram (30 mmole) S-(-)-α-xylylamine processing, gained solution inserts the crystal seed of the superfine salt that parses in advance, 25 ℃ leave standstill 8 hours after, the white solid that generates is leached, wash with ether, at air drying, obtain the rough title compound of 4.78 grams, its fusing point: be 137-140 ℃.
8.87 gram crude products are dissolved in 200 milliliters of acetonitriles through backflow, be chilled to 25 ℃ again and carry out recrystallization, left standstill 1 hour, leach crystal at 25 ℃, after acetonitrile and ethyl acetate washing, at air drying, obtain 6.81 gram title compounds, its fusing point: be 144～146 ℃, 6.81 gram samples are carried out the recrystallization second time with 150 milliliters of acetonitriles by method last time, obtain 6.02 gram title compounds, its fusing point is 146～147 ℃, (α)
D=-4.5 ° (C=2.0, methyl alcohol).
B) N-(tertbutyloxycarbonyl)-the L-3-hydroxyvaline
The N-(tertbutyloxycarbonyl)-L-3-hydroxyvaline, α-methylbenzyl amine salt (6.02 grams, 17.0 mmoles) separate with mixed solution one oscillates of 250 milliliters of ethyl acetate and 100 milliliter of 10% potassium hydrogen sulfate solution and by layer.Organic layer water and salt water washing, dry (using sodium sulfate) also flashes to foam-like material, adds the hexane porphyrize, obtains a kind of title compound 3.79 grams of free-pouring white powder, and its fusing point is 116～118 ℃, (α)
D=+7.6 ℃ (C=2.0 ethyl acetate).
The sample of this title compound can change its methyl esters with diazomethane into.5 milligrams of methyl esters and 10 milligram of three (the 3-(seven fluorine third hydroxyl methylene radical)-d-camphor (CamPhorato)) mixture of europium (III), the proton magnetic resonance (PMR) in the time of 0 ℃ (400 megahertz) demonstrates, and the ratio of their enantiomorphs is 95: 5.Become its free amino group acid hydrochloride after this compound (with hydrochloric acid/ethyl acetate) gone to protect.With specific rotation shown on the document relatively: after reach a conclusion; The stereochemistry absolute configuration of this compound belongs to S configuration (see Bull.Chem.SoC, Japan, 39,2287(1966)).
C) N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-L-3-hydroxyl valine amide
According to the step of example 1A, and use the N-(tertbutyloxycarbonyl)-L-3-hydroxyvaline replacement N-(tertbutyloxycarbonyl)-D, the L-3-hydroxyvaline then generates title compound.
D) (3S)-and 3-((tertbutyloxycarbonyl) amino)-4,4-dimethyl-1-(benzyloxy)-the 2-azetidinone
According to the step of routine 1B of examination and 1C, and use the N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-L-3-hydroxyl valine amide replaces the N-(tertbutyloxycarbonyl)-N
2-(benzyloxy)-D, L-3-hydroxyl valine amide makes title compound.The flash chromatography that mother liquor after the crystallization is made with LPS-1 silica gel is made with extra care (moving phase is 20% ethyl acetate/normal hexane).
E) (3S)-and 3-((tertbutyloxycarbonyl) amino)-1-hydroxyl-4,4-dimethyl-2-azetidinone
Step according to example 1D, and use (3S)-3-((tertbutyloxycarbonyl) amino)-4,-4-dimethyl-1-(benzyloxy)-2-azetidinone replacement (3 ±)-3-((tertbutyloxycarbonyl) amino)-4,4-dimethyl-1-(benzyloxy)-and the 2-azetidinone, make title compound.
F) (3S)-and 3-((tertbutyloxycarbonyl) amino)-2-oxygen base-4,4-dimethyl-1-azelidinyl vitriol sylvite.
Step according to example 1E, and use (3S)-3-((tertbutyloxycarbonyl) amino)-1-hydroxyl-4,4-dimethyl-2-azetidinone replaces (3 ±)-3-((tertbutyloxycarbonyl) amino)-1-hydroxyl-4, and 4-dimethyl-2-azetidinone makes title compound.After removing volatile matter, rough residue is dissolved in the damping fluid (PH is 7.2) of acetone/0.5M potassium primary phosphate of 10%, pH value transferred to 5.0 with the 3N potassium hydroxide solution.This solution with chromatography in DoWex(potassium type) on separate, refining on HP-20 with chromatography then.
G) (3S(Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene) amino) oxygen base) acetate, benzhydryl ester, sodium salt
(Z)-(2-amino-4-thiazolyl) ((the 2-two benzyloxies-2-oxygen oxyethyl group) imido grpup) acetate of 1.152 grams (2.81 mmole) is dissolved in 9.4 milliliters of dimethyl formamides, again diisopropylethylamine (0.54 milliliter, 3.09 mmoles) is added.This mixture is cooled to-20 ℃, adds chlorinated diphenyl phosphate (0.59 milliliter, 2.81 mmoles) again.The mixture that generates was stirred 1 hour, obtain a kind of mixed anhydride.
Again with (3S)-3-((tertbutyloxycarbonyl) amino)-2-oxygen base-4,4-dimethyl-1-azelidinyl vitriol, sylvite (0.98 gram, 2.81 mmoles) are suspended in 7.5 milliliters of trichloromethanes, be chilled to-10 ℃ and add methyl-phenoxide (2.13 milliliters), and then add 9.4 milliliters of trifluoroacetic acids.This mixture was stirred 1 hour down at-10 ℃, add toluene (about 5 milliliters), volatile matter is removed in evaporation.Residue obtains a kind of white powder (3S)-amino-2-oxygen base-4 through vacuum-drying, 4-dimethyl-1-azelidinyl vitriol with normal hexane and anhydrous diethyl ether, grinding.
Residue is chilled to-20 ℃, is dissolved in 9.4 milliliters of dimethyl formamides, add diisopropylethylamine (1.47 milliliters, 8.34 mmoles), add mixed anhydride then immediately.Reaction mixture was stirred 3 hours at-20 ℃, remove volatile matter in a vacuum, the gained residue is dissolved under 0 ℃ in 20% aqueous acetone solution, with aqueous carbonic acid hydrogen sodium its pH value is transferred to 6.5.
The mixture of last gained is refining with column chromatography.Be stationary phase with Dowex50x2-400 resin (sodium type) earlier, 20% aqueous acetone solution is that moving phase is refining; Thereupon, be that stationary phase (moving phase is water, 5%, 10%, 20%, 30% and 40% aqueous acetone solution) carries out chromatographic refining with HP-20, obtain title compound.
H) (3S(Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-3-azelidinyl) amino)-2-oxo ethylidene) amino) oxygen base) acetate, disodium salt
With (3S(Z))-2-(((1-(2-amino-4-thiazolyl)-2-((2,2-dimethyl-4-Oxy-1-(sulphur oxygen base)-azelidinyl) amino)-and 2-oxo ethylidene) amino) the oxygen base) acetate, benzhydryl ester, sodium salt is suspended in 11.2 milliliters-10 ℃ the methylene dichloride, add methyl-phenoxide (1.12 milliliters), subsequently, drip 18.7 milliliters of trifluoracetic acids, mixture stirred 40 minutes down at 0 ℃.Add toluene, evaporate and remove volatile matter, this residue grinds with anhydrous diethyl ether, obtains a kind of white solid after the vacuum-drying.In this residue water-soluble (PH is 2.75), with HP-20 stationary phase, with chromatography refining (moving phase is water, 5%, 10%, 20% aqueous acetone solution), obtain the zwitter-ion of 640 milligrams of title compounds through freeze-drying.Zwitter-ion is soluble in water, add the normal sodium bicarbonate of its twice (244 milligrams, 2.9 mmoles), solution PH is 5.75.With HP-20 is stationary phase (water is moving phase), and this solution is carried out chromatographic separation, obtains 572 milligrams of title compounds through freeze-drying, and its fusing point is 140～145 ℃
To C
12H
13N
5O
9S
2Na
21.56H
2O analyzes and calculates:
C，28.31，H，3.10;N，13.64
Measure: C, 28.31, H, 3.19; N, 13.76
Claims (4)
1, a kind of method for preparing aza cyclobutanone compound, this compound is shown below:
This method comprises with the complex compound shown in the following formula:
With the compound sulfonation shown in the following formula:
The compound of gained is shown below:
Wherein A is benzyloxycarbonyl, or tertbutyloxycarbonyl,
R
1And R
2Be methyl;
R
3Be benzyl;
M is 0,1,2 or 3,
Use alkaline purification then, make the cyclisation of gained compound.
2, according to the method described in the claim 1, the complex compound that wherein is used for sulfonation reaction is the pyridine sulphur trioxide.
3, according to the method described in the claim 1, wherein A is a tertbutyloxycarbonyl.
4, according to the method described in the claim 1, wherein A is a tertbutyloxycarbonyl; R
1And R
2It all is methyl; R
3It is benzyl; The complex compound that is used for sulfonation reaction is the pyridine sulphur trioxide.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US695,775 | 1985-01-28 | ||
| US06/695,775 US4638061A (en) | 1985-01-28 | 1985-01-28 | [3S(Z)]-2-[[[1-(2-amino-4-thiazolyl)-2-[[2,2-dimethyl-4-oxo-1-(sulfooxy)-3-azetidinyl]amino]-2-oxoethylidene]-amino]oxy] acetic acid and intermediate |
| CN86100736A CN1014894B (en) | 1985-01-28 | 1986-01-28 | Process for preparing 4,4-dialkyl-2-azetidinones |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN86100736A Division CN1014894B (en) | 1985-01-28 | 1986-01-28 | Process for preparing 4,4-dialkyl-2-azetidinones |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1055736A true CN1055736A (en) | 1991-10-30 |
| CN1018824B CN1018824B (en) | 1992-10-28 |
Family
ID=25742172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 91103499 Expired CN1018824B (en) | 1985-01-28 | 1986-01-28 | Process for preparing 4,4-dialkyl-2-azetidinones |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1018824B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103408635A (en) * | 2013-06-27 | 2013-11-27 | 深圳翰宇药业股份有限公司 | Method for synthesizing mifamurtide |
| CN113754651A (en) * | 2020-06-02 | 2021-12-07 | 中国医学科学院医药生物技术研究所 | Beta-lactam compound, application and preparation method thereof |
| CN114085170A (en) * | 2021-11-23 | 2022-02-25 | 山东永浩新材料科技有限公司 | Preparation method of lithium alkyl sulfate |
-
1986
- 1986-01-28 CN CN 91103499 patent/CN1018824B/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103408635A (en) * | 2013-06-27 | 2013-11-27 | 深圳翰宇药业股份有限公司 | Method for synthesizing mifamurtide |
| CN113754651A (en) * | 2020-06-02 | 2021-12-07 | 中国医学科学院医药生物技术研究所 | Beta-lactam compound, application and preparation method thereof |
| WO2021244199A1 (en) * | 2020-06-02 | 2021-12-09 | 中国医学科学院医药生物技术研究所 | β-LACTAM COMPOUND, USE THEREOF AND PREPARATION METHOD THEREFOR |
| CN113754651B (en) * | 2020-06-02 | 2023-04-18 | 中国医学科学院医药生物技术研究所 | Beta-lactam compound, application and preparation method thereof |
| CN114085170A (en) * | 2021-11-23 | 2022-02-25 | 山东永浩新材料科技有限公司 | Preparation method of lithium alkyl sulfate |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1018824B (en) | 1992-10-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1147502C (en) | Method for large-scale production of Di (uridine 5'-tetraphosphate) and salts thereof | |
| CN1071745C (en) | Process for the synthesis of azetidinones | |
| CN1249744A (en) | Nitric oxide synthase inhibitors | |
| CH657610A5 (en) | 1-SULFO-2-OXOAZETIDINE DERIVATIVES, THEIR PRODUCTION AND THE PHARMACEUTICAL PREPARATIONS CONTAINING THE SAME. | |
| CN1176080C (en) | Indeno-, naphtho-, and benzocyclohepta-dihydrothiazole derivatives, the production thereof and their use as anorectic medicaments | |
| CN1029956C (en) | Process for resoluting folinic acid | |
| CN1040002C (en) | Diastereoisomer of 3-cephem-4-carbonic acid-1-(isopropxycarbonyloxy) ethylester and process for preparing same | |
| CN1014894B (en) | Process for preparing 4,4-dialkyl-2-azetidinones | |
| CN1055736A (en) | 4, the preparation method of 4-dialkyl group-2-azetidinones | |
| CN1365362A (en) | Process for the preparation of basic anti-biotic-inorganic acid and intermediate oxalates | |
| CN87106996A (en) | Quinoline compound, their preparation method and with its carcinostatic agent as the active drug component | |
| CN100351261C (en) | Crystalline glucosamine sulphate metal salts and its preparation method | |
| CN86102630A (en) | The method for preparing 7-amino-3-propenylcephalosporanic acid and ester class thereof | |
| CN1310898C (en) | Taxinol water soluble derivative | |
| EP0000645B1 (en) | Isopenicillins, processes for their preparation, and compositions containing them | |
| CN1393446A (en) | Fused pyrazole compound | |
| CN1083476A (en) | The fumarate of quinoline | |
| Sumi et al. | The stereocontrolled synthesis of versatile carbapenem intermediates using the Barton O-acyl 2-thiophyridylhydroxamate fragmentation | |
| DE69816057T2 (en) | ANTIBACTERIAL SUBSTITUTED 7-ACYLAMINO-3- (METHYLHYDRAZONO) METHYL-CEPHALOSPORINE AND INTERMEDIATE PRODUCTS | |
| EP0123442A1 (en) | Improvements in or relating to a process for producing beta-lactam compounds | |
| US4767851A (en) | Process for the preparation of 7-amino and 7-substituted amino-desacetoxycephalosporins | |
| CN1021225C (en) | Hydrate of penicillin derivative and process for preparing same | |
| CN1067055A (en) | The crystallinity acid salt of 3-cephalo-4-carboxylic acid-1-(2,2-dimethyl propylene acyloxy) ethyl ester diastereomer | |
| EP0122002B1 (en) | Process for preparing azetidinone derivatives | |
| DD232490A5 (en) | PROCESS FOR PREPARING 1-SULOFO-2-AZETIDINONE DERIVATIVES |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| C13 | Decision | ||
| GR02 | Examined patent application | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |