CN103193791B - A kind of synthetic method of medicinal artemisinin - Google Patents

A kind of synthetic method of medicinal artemisinin Download PDF

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CN103193791B
CN103193791B CN201310100675.9A CN201310100675A CN103193791B CN 103193791 B CN103193791 B CN 103193791B CN 201310100675 A CN201310100675 A CN 201310100675A CN 103193791 B CN103193791 B CN 103193791B
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dihydroartemisinic acid
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CN103193791A (en
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张万斌
刘德龙
袁乾家
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Shanghai Jiaotong University
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/12—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
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Abstract

The present invention discloses a kind of high-efficiency synthesis method of medicinal artemisinin; comprise the steps: dihydroartemisinic acid by obtaining dihydroartemisinic acid derivative to the protection of carboxyl; it is become corresponding peroxidation dihydroartemisinic acid derivative by peroxide oxidation in the presence of a catalyst, then can obtain target product Artemisinin with high yield under the catalysis of acid with under oxygen effect.Compared with prior art, tool of the present invention has the following advantages: agents useful for same is cheaply easy to get, and synthetic route is short, and reaction preference is high, and preparation process is environmentally friendly, and simply, total recovery is high for operation and aftertreatment, is applicable to suitability for industrialized production.

Description

A kind of synthetic method of medicinal artemisinin
The application is application number is 201210181561.7, and the applying date is 2012.6.5, and denomination of invention is the divisional application of " a kind of method being prepared Artemisinin by arteannuinic acid ".
Technical field
The present invention relates to biomedicine field, specifically refer to a kind of preparation method relating to anti-malarial class drug artemisinin.
Background technology
Artemisinin (Artemisinin), the sesquiterpene lactones anti-malarial class medicine having peroxy-radical extracted from Chinese medicine Herba Artemisiae annuae is that Chinese first of finding is by internationally recognized natural drug.The antimalarial mechanism of Artemisinin is different from other antimalarial drug, and its Main Function is by disturbing plasmodial pellicle-mitochondrial function, but not interfere with folate metabolism, thus cause polypide structure all to be disintegrated.In addition, take Artemisinin as raw material, also can synthesize its derivative multiple, as dihydroarteannuin, Artemether, Artesunate etc.Low, the anti-cruel property of these artemisinin-based drug toxicity is strong, is approved as the choice drug of world wide internal therapy encephalic malaria and pernicious malaria by WTO.
Current medicinal artemisinin is separated to obtain from the leaf of Chinese medicine sweet wormwood and feverfew Herba Artemisiae annuae and bud.Due to buying, the results of sweet wormwood, until factory process is extracted, link is more, waste time and energy, and different acquisition ground and different acquisition phase sweet wormwood quality have very large difference, simultaneously, a large amount of collection natural resources, will inevitably welding and the eubiosis, causes resource exhaustion.Therefore, be increase the resource of Artemisinin, the development research carrying out Artemisinin and derivative thereof is all being stepped up in countries in the world, and supplying Artemisinin steadily in the long term and in large quantities becomes the baptism that various countries scientist faces.So the chemosynthesis of exploitation Artemisinin, not only economizes on resources, environmentally friendly, can also reduce the drug cost of patient simultaneously, more effectively suppress the harm that malaria causes the mankind.
Patent US4992561 take dihydroartemisinic acid as raw material, adopts photochemical method to introduce peroxide bridge.Due to the restriction of photochemistry self, as complex operation, unsuitable scale operation, is therefore difficult to realize suitability for industrialized production.It is the method that raw material carrys out synthetic artemisinin that document (Tetrahedron, 1986,42,819-828) reports use (R)-(+)-Vanillin, however due to synthetic route long, total recovery is low, and Atom economy is poor.In addition be also adopt photochemical method to introduce peroxide bridge, be difficult to realize suitability for industrialized production.What other were reported as MitchellA.Avery (J.Am.Chem.Soc., 1992.114.974-979) utilizes pulegone for Material synthesis Artemisinin, and its synthetic route is longer, yield is low.Utilize ozone to introduce peroxide bridge, operational difficulty, security is poor, and industrial prospect is not high simultaneously.If utilize traditional chemical synthesis process to realize the introducing of peroxide bridge, not only workable, also very likely test suitability for industrialized production.Document (J.Am.Chem.Soc., 1964,86,3880, J.Am.Chem.Soc., 1968,90,975) utilizes oxygen to produce singlet oxygen, and then photochemical method also can be replaced to realize the introducing of peroxide bridge under being reported in certain catalyzer existence.Patent WO2009088404 once reported that through Sodium orthomolybdate be catalyzer, was that peroxide bridge introduced by oxygenant with hydrogen peroxide.But its selectivity of product obtained is poor, by product is many, causes the total recovery of final Artemisinin low (<20%), is also difficult to realize suitability for industrialized production.
In sum, it is long that the existing preparation method about Artemisinin also exists synthetic route, complex operation, and Atom economy is poor, and overall yield is low, is unfavorable for environmental protection and suitability for industrialized production.
Summary of the invention
Object of the present invention be exactly in order to overcome that defect that prior art exists provides a kind of rational technology, simple to operate and with low cost and total recovery high the preparation method of Artemisinin.
Object of the present invention can be achieved through the following technical solutions:
The present invention relates to a kind of synthetic method of medicinal artemisinin, specifically refer to by the synthetic technology of arteannuinic acid to Artemisinin.The method is by following two kinds of routes, any one realizes:
Route one:
The first step: take arteannuinic acid as starting raw material, under the condition of catalyzer/hydrogen or nickelous chloride/sodium borohydride, obtains dihydroartemisinic acid 2 through reduction reaction in organic solvent;
Second step: in dihydroartemisinic acid 2 organic solvent superoxide and metal catalyst effect under obtain peroxidation dihydroartemisinic acid 3 through peroxidation;
3rd step: peroxidation dihydroartemisinic acid 3 reacts also purifying through acid catalyzed rearrangement in organic solvent and obtains target compound Artemisinin 1.
Route two:
The first step: take arteannuinic acid as starting raw material, under the condition of catalyzer/hydrogen or nickelous chloride/sodium borohydride, obtains dihydroartemisinic acid 2 through reduction reaction in organic solvent;
Second step: dihydroartemisinic acid 2 is in organic solvent by obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl;
3rd step: dihydroartemisinic acid derivative 4 obtains corresponding peroxidation dihydroartemisinic acid derivative 5 with under the effect of superoxide and metal catalyst through peroxidation in organic solvent;
4th step: peroxidation dihydroartemisinic acid derivative 5 reacts also purifying through acid catalyzed rearrangement in organic solvent and obtains target compound Artemisinin 1.
Route of the present invention is as follows:
In above-mentioned two kinds of routes, described arteannuinic acid refers to: the by-product form in Artemisinin leaching process or the arteannuinic acid obtained by fermentation process.
In above-mentioned two kinds of routes, catalyzer used in the reduction reaction of described arteannuinic acid comprises the palladium or palladium hydroxide that are carried on charcoal, be carried on the rhodium of aluminium sesquioxide, Raney nickel, all catalyzer that can be used for this reaction such as platinum oxide, the mol ratio of arteannuinic acid and catalyzer is 1:0.01 ~ 1, the solvent of reaction can for comprising methyl alcohol, ethanol, propyl alcohol, Virahol, propyl carbinol, isopropylcarbinol, tetrahydrofuran (THF), all polarity and non-polar solvents that can be used for this reaction such as toluene, particular methanol, the pressure reacting hydrogen used is 1 ~ 100bar, preferred 50bar, temperature of reaction is-50 ~ 60 DEG C, preferably 25 DEG C.
In above-mentioned two kinds of routes, in the reduction reaction of described arteannuinic acid under the condition of nickelous chloride/sodium borohydride, solvent can for comprising methyl alcohol, ethanol, propyl alcohol, Virahol, all polarity and non-polar solvents that can be used for this reaction such as propyl carbinol, isopropylcarbinol, tetrahydrofuran (THF), toluene, particular methanol, the mol ratio of arteannuinic acid and nickelous chloride, sodium borohydride is 1:0.01 ~ 10:1 ~ 20, and temperature of reaction is-50 ~ 60 DEG C, preferably-40 DEG C.
In above-mentioned route two step 2, described refers under alkalescence exists to carboxy protective, dihydroartemisinic acid 2 is in organic solvent through obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl, wherein: dihydroartemisinic acid 2 is 1:(1 ~ 30 with the consumption mol ratio of alkali), temperature of reaction is-50 ~ 60 DEG C; Described alkali is all mineral alkali or organic basess of can be used for this reaction.
In above-mentioned route two; described dihydroartemisinic acid is in organic solvent through obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl, and wherein R-can be alkyl, thiazolinyl, alkynyl, aryl, cycloalkyl group, formic acid ester group, all groups that may be used for protection carboxyl such as MOM, TMS, THP, Ac, Ms, Ts, Bz, Piv, TES, TBS or TBDPS.Protection reagent used is the reagent of the applicable carboxy protective of corresponding halogenide or other form; as methyl iodide, diazomethane, methoxymethyl chlorine, methyl-chloroformate, Vinyl chloroformate, chloroformic acid-2; 2,2-trichloro ethyl ester, trimethyl silicon based chlorine, the chloro-tetrahydropyrans of 2-, Acetyl Chloride 98Min., methylsulfonyl chloride, Tosyl chloride, benzyl chloride, bromotoluene, valeryl chlorine, the silica-based chlorine of triethyl, t-Butyldimethylsilyl chlorine, the silica-based chlorine of tert-butyl diphenyl.Dihydroartemisinic acid is 1:1 ~ 10 with the mole dosage ratio of protection reagent.(wherein MOM is methoxyl methyl; TMS is trimethyl silicon based; THP is THP trtrahydropyranyl, and Ac is ethanoyl, and Ms is methylsulfonyl; Ts is p-toluenesulfonyl; Bz is benzoyl, and Piv is valeryl, and TES is that triethyl is silica-based; TBS is t-Butyldimethylsilyl, and TBDPS is that tert-butyl diphenyl is silica-based).
Further, wherein alkyl refers to have C nh 2n+1general structure, the aliphatic group of straight or branched, n=1 ~ 8, as methyl, ethyl, propyl group, sec.-propyl, 2-methyl isophthalic acid-propyl group, 2-methyl-2-propyl, 2-methyl-1-butene base, 3-methyl isophthalic acid-butyl, 2-methyl-3-butyl, 2, 2-dimethyl-1-butyl, 2-methyl-1-pentene base, 3-methyl-1-pentene base, 4-methyl-1-pentene base, 2-methyl-2 amyl group, 3-methyl-2-amyl group, 4-methyl-2-amyl group, 2, 2-dimethyl-1-butyl, 3, 3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl, amyl group, hexyl, heptyl, the straight or branched alkyl such as octyl group.Thiazolinyl refers to the alkyl of the straight or branched containing one or more carbon-carbon double bond, C 2~ C 8thiazolinyl comprises vinyl, allyl group, butenyl, pentenyl, hexenyl, butadienyl, piperylene base, oneself straight or branched alkyl such as two thiazolinyls, 2-ethyl hexyl thiazolinyl.Alkynyl refers to the alkyl of the straight or branched containing one or more carbon-carbon triple bond, C 2~ C 8alkynyl comprises ethynyl, the straight or branched alkyl such as proyl, butynyl, pentynyl, hexin base, valerylene base, 5-methyl-2-heptyne base.Aryl refers to the aryl or assorted aryl that comprise monocycle or many rings, as phenyl, naphthyl, anthryl, phenanthryl, dibiphenylyl, terphenyl, three base phenmethyls, phenmethyl, 2-menaphthyl, 9-anthracene ethyl, 9-luxuriant and rich with fragrance methyl, 3-diphenyl ethyl, pyrryl, furyl, thienyl, pyridyl, benzofuryl, benzothienyl, indyl, quinolyl, isoquinolyl, wherein can with a multiple substituting group on aromatic ring.Cycloalkyl group refers to and comprises one or more ring, saturated or undersaturated alkyl, as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, suberyl, two cyclic terpene bases, cyclobutene base, cyclopropenyl radical, cyclopentenyl, cyclohexenyl, wherein can with one or more substituting group on ring.
In the second step of above-mentioned route two, solvent for use comprises tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, tetracol phenixin, Virahol, all conventional organic solvents that can be used for this reaction such as DMF, DMSO, preferred methylene dichloride, its consumption is 100 ~ 5000mL/ mole, temperature of reaction is-50 ~ 60 DEG C, preferably 25 DEG C.Alkali used comprises mineral alkali or the organic bases that cesium carbonate, salt of wormwood, sodium carbonate, sodium bicarbonate, saleratus, triethylamine, diisopropylethylamine, pyridine, imidazoles etc. can be used for this reaction.
In above-mentioned two kinds of routes, in described oxidizing reaction: solvent for use comprises the conventional organic solvent that acetone, tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, Virahol, DMF, DMSO, benzene etc. can be used for this reaction, its consumption is 50 ~ 10000mL/ mole, temperature of reaction is-78 ~ 60 DEG C, preferable temperature-40 DEG C.
In above-mentioned two kinds of routes, in described oxidizing reaction: metal catalyst comprises calcium, sodium, molybdenum, chromium, lanthanum, cerium, tungsten, scandium, titanium, zirconium, the salt of vanadium and oxide compound, as phospho-molybdic acid, chromium trioxide, chromium chloride, potassium bichromate, calcium chloride, Losantin, Tungsten oxide 99.999, sodium wolframate, Scium trioxide, Scium trinitrate, Scium trichloride, zirconium dioxide, zirconium oxychloride, vanadium oxide, vanadic acid sodium, cerous nitrate, ceric sulfate, cerium oxide, Cerium II Chloride, cerous hydroxide, lanthanum-cerium chloride, Phosbloc cerium, lanthanum trioxide, Lanthanum trichloride, lanthanum hydroxide, lanthanum nitrate, Phosbloc, lanthanum fluoride, lanthanum hexaborane, clorox, all catalyzer that can be used for this reaction such as sodium perchlorate, the mol ratio of catalyzer and compound 2 or 4 is 1:1 ~ 100.
In above-mentioned two kinds of routes, in described oxidizing reaction: alkali comprises cesium carbonate, salt of wormwood, sodium carbonate, sodium bicarbonate, saleratus, sodium hydroxide, potassium hydroxide, lithium hydroxide, triethylamine, diisopropylethylamine, pyridine, imidazoles, 1,8-diazabicyclo [5.4.0] 11 carbon-7-alkene, 1,4-diazabicyclo [2.2.2] octane, Dicyanodiamide, tetramethyl guanidine, Sulphaguanidine, N, N, N', N'-Tetramethyl Ethylene Diamine etc. can be used for mineral alkali or the organic bases of this reaction.The mol ratio of compound 2 or 4 and alkali is 1:0.01 ~ 10.
In above-mentioned two kinds of routes, in described oxidizing reaction: superoxide comprises the superoxide that metachloroperbenzoic acid, hydrogen peroxide, peroxy tert-butyl alcohol, Peracetic Acid, peroxy trifluoroacetic acid etc. can be used for this reaction, wherein hydrogen peroxide comprises the aqueous hydrogen peroxide solution of 30%, 50% and 70%, the preferably aqueous hydrogen peroxide solution of 30%, the mol ratio of compound 2 or 4 and superoxide is 1:1 ~ 100.
In above-mentioned two kinds of routes, in described acid catalyzed reaction: solvent comprises the conventional organic solvent that acetone, tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, Virahol, sherwood oil, hexanaphthene, normal hexane, DMF, DMSO, n-propyl alcohol, propyl carbinol, ethyl acetate, benzene etc. can be used for this reaction, its consumption is 50 ~ 10000mL/ mole, and temperature of reaction is-78 ~ 60 DEG C.
In above-mentioned two kinds of routes, in described acid catalyzed reaction: acid comprises p-methyl benzenesulfonic acid, trifluoroacetic acid, acetic acid, camphorsulfonic acid, copper trifluoromethanesulfcomposite, aluminum chloride, iron trichloride, cupric chloride, cupric oxide, ferric oxide, Cu/Dowex resin and Cu (Tc) 2(thiophene-2-carboxylic acid copper) etc. all can be used for the Bronsted acid of this reaction or Lewis sour.The mol ratio of acid used and peroxidation dihydroartemisinic acid 3 or peroxidation dihydroartemisinic acid derivative 5 is 1:1 ~ 100.
In above-mentioned two kinds of routes, described purification process, comprises column chromatography and recrystallization.Column chromatography and recrystallization solvent for use comprise conventional inorganic solvent and the organic solvents such as water, ethanol, methyl alcohol, Virahol, hexanaphthene, ether, methylene dichloride, isopropyl ether, methyl tertiary butyl ether, toluene, sherwood oil, acetone, ethyl acetate, normal hexane.
In the present invention, the synthetic route of employing has the following advantages:
1. with by product in Artemisinin leaching process or the arteannuinic acid that obtained by fermentation process for starting raw material, after reduction, obtain pure white solid dihydroartemisinic acid 2, after optimizing, productive rate can reach 99%.This reaction stereoselectivity is good, and product purity is high, and reaction yield is high, is easy to scale operation.
2. dihydroartemisinic acid 2 obtains corresponding superoxide 3 through peroxidation, reacts and directly can drop into next step reaction after simple process.The traditional chemical process of this reaction introduces peroxide bridge, and mild condition is easy and simple to handle.Utilize method provided by the present invention, the regioselectivity of reaction is better, and productive rate is high, is applicable to suitability for industrialized production simultaneously.
3. superoxide 3 obtains compound 1 through acid catalyzed rearrangement.This operation is easy, and agents useful for same is cheap, and mild condition, productive rate is high, and whole route is suitable for suitability for industrialized production.
4. dihydroartemisinic acid 2 is through obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl.Agents useful for same is cheap, and reaction conditions is gentle, convenient post-treatment, and productive rate is high, and product does not need purifying directly can drop into next step reaction.
5. dihydroartemisinic acid derivative 4 obtains corresponding peroxidation dihydroartemisinic acid derivative 5 through peroxidation, and product directly can drop into next step reaction after simple process.The traditional chemical process of this reaction introduces peroxide bridge, and mild condition is easy and simple to handle.Utilize method provided by the present invention, the regioselectivity of reaction is better, and productive rate is high, is applicable to suitability for industrialized production simultaneously.
6. peroxidation dihydroartemisinic acid derivative 5 obtains compound 1 through acid catalyzed rearrangement.This reaction agents useful for same is cheap, and mild condition, convenient post-treatment, productive rate is high, and whole route is applicable to suitability for industrialized production.
Compared with prior art, preparation method's agents useful for same of the Artemisinin that the present invention relates to cheaply is easy to get, and synthetic route is short, and reaction preference is high, and preparation process is environmentally friendly, and simply, total recovery is high, is more suitable for suitability for industrialized production for operation and aftertreatment.
Embodiment
The present invention can contrast following specific embodiment, and the invention will be further described, but the present invention is not limited to following examples.
Embodiment 1
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (4.3mmol) join in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), potassium bichromate (4.2mmol), salt of wormwood (4.2mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, extract by ethyl acetate (500mL × 3).Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.Crude product re-crystallizing in ethyl acetate, obtains colourless acicular crystal 57g, three step total recoverys 47%.
Embodiment 2
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), sodium perchlorate (424mmol), pyridine (424mmol) join in 1000mL acetone.At-78 DEG C, reaction mixture slowly drips the hydrogen peroxide (4.2mol) of 30%, and reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3, add acetic acid (4.2mol).Revolve after reaction carries out 3 hours and steam removing organic solvent, extract by ethyl acetate (500mL × 3).Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 60g, three step total recoverys 50%.
Embodiment 3
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), clorox (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, camphorate sulfonic acid (42mmol) in hexanaphthene (500mL) solution of peroxidation dihydroartemisinic acid 3.Revolve after reaction carries out 3 hours and steam removing organic solvent, extract by ethyl acetate (500mL × 3).Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 59g, three step total recoverys 49%.
Embodiment 4
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL ethanol, 25 DEG C, in atmosphere of hydrogen (50bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), vanadic acid sodium (420mmol), saleratus (420mmol) join in 1000mL Virahol.At 25 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in hexanaphthene (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (42mmol), revolve after reaction carries out 3 hours and steam removing organic solvent.Residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 77g, three step total recoverys 56%.
Embodiment 5
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams except organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), phospho-molybdic acid (424mmol), cesium carbonate (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol), revolve after reaction carries out 3 hours and steam removing organic solvent.With ethyl acetate (500mL × 3) extraction, merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 70g, three step total recoverys 58%.
Embodiment 6
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (4.3mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Scium trioxide (424mmol), sodium hydroxide (4.2mol) join in 1000mL n-propyl alcohol.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in sherwood oil (500mL) solution of peroxidation dihydroartemisinic acid 3, add aluminum chloride (4.2mol).Revolve after reaction carries out 3 hours and steam removing organic solvent, extract by ethyl acetate (500mL × 3).Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 69g, three step total recoverys 57%.
Embodiment 7
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (427mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), sodium wolframate (424mmol), 1,8-diazabicyclo [5.4.0] 11 carbon-7-alkene (4.2mol) join in 1000mL tetrahydrofuran (THF).At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add aluminum chloride (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 54g, three step total recoverys 45%.
Embodiment 8
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, (1bar)-50 DEG C reaction 24 hours in atmosphere of hydrogen.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), lanthanum nitrate (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, camphorate sulfonic acid (42mmol) in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3.Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 61g, three step total recoverys 51%.
Embodiment 9
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), lanthanum trioxide (42mmol), triethylamine (420mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 70g, three step total recoverys 58%.
Embodiment 10
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL propyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), cerous hydroxide (424mmol), sodium carbonate (4.2mol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 72g, three step total recoverys 60%.
Embodiment 11
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (43mmol) join in 1000mL ethanol, and in room temperature atmosphere of hydrogen, (50bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Lanthanum trichloride (42mmol), sodium hydroxide (420mmol) join in 25mL propyl carbinol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 64g, three step total recoverys 53%.
Embodiment 12
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (4.3mmol) join in 1000mL methyl alcohol, 25 DEG C, in atmosphere of hydrogen (100bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), chromium trioxide (4.2mmol), potassium hydroxide (420mmol) join in 1000mL methyl alcohol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add iron trichloride (420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 60g, three step total recoverys 50%.
Embodiment 13
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), Lanthanum trichloride (4.2mmol), sodium hydroxide (420mmol) join in 1000mL toluene.At 60 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 66g, three step total recoverys 55%.
Embodiment 14
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), chromium chloride (424mmol), tetramethyl guanidine (424mmol) join in 20000mL benzene.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid, Cu/Dowex (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 71g, three step total recoverys 59%.
Embodiment 15
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL methyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), clorox (424mmol), imidazoles (42mmol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in ether (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid Diethyl ether recrystallization, obtains colourless acicular crystal 63g, three step total recoverys 52%.
Embodiment 16
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (4.3mmol) join 1000mL1, in 4-dioxane ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), zirconium oxychloride (4.2mmol), potassium hydroxide (4.2mmol) join in 1000mL ethyl acetate.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add Cu (Tc) 2(42mmol).Revolve after reaction carries out 6 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 59g, three step total recoverys 49%.
Embodiment 17
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), lanthanum nitrate (420mmol), salt of wormwood (420mmol) join in 1000mL propyl alcohol.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, add copper trifluoromethanesulfcomposite (4.2mol) in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3.Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 69g, three step total recoverys 57%.
Embodiment 18
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd (OH) 2/C (4.3mmol) join in 1000mL methyl alcohol, 25 DEG C, in atmosphere of hydrogen (100bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), zirconium hydroxide (4.2mmol), triethylamine (420mmol) join in 1000mL ethanol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extraction, merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 61g, three step total recoverys 51%.
Embodiment 19
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Losantin (424mmol) join in 1000mL ethanol.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 10 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 69g, three step total recoverys 57%.
Embodiment 20
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), lanthanum-cerium chloride (424mmol), cesium carbonate (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methyl alcohol (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 65g, three step total recoverys 54%.
Embodiment 21
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL propyl carbinol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), Tungsten oxide 99.999 (4.2mmol), N, N, N', N'-Tetramethyl Ethylene Diamine (4.2mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in normal hexane (500mL) solution of peroxidation dihydroartemisinic acid 3, add cupric chloride (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid sherwood oil recrystallization, obtains colourless acicular crystal 67g, three step total recoverys 56%.
Embodiment 22
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), Phosbloc cerium (4.2mmol), lithium hydroxide (4.2mmol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 66g, three step total recoverys 55%.
Embodiment 23
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (4.3mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), vanadium oxide (424mmol), pyridine (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in sherwood oil (500mL) solution of peroxidation dihydroartemisinic acid 3, add cupric oxide (4.2mol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 64g, three step total recoverys 53%.
Embodiment 24
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), lanthanum nitrate (424mmol), sodium hydroxide (4.2mol) join in 1000mL methyl alcohol.At 60 DEG C, in system, slowly add metachloroperbenzoic acid (42mol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid Isosorbide-5-Nitrae-dioxane recrystallization, obtains colourless acicular crystal 71g, three step total recoverys 59%.
Embodiment 25
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), clorox (420mmol) join in 1000mL propyl alcohol.At-78 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 61g, three step total recoverys 51%.
Embodiment 26
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), cerous hydroxide (42mmol), triethylamine (424mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 70g, three step total recoverys 58%.
Embodiment 27
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (43mmol) join in 1000mL ethanol, and in room temperature atmosphere of hydrogen, (50bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), clorox (42mmol), sodium hydroxide (420mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly add peroxy tert-butyl alcohol (4.2mol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in trichloromethane (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 72g, three step total recoverys 60%.
Embodiment 28
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methyl alcohol, react 24 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Phosbloc (424mmol), diisopropyl ethyl amine (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 10 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 67g, three step total recoverys 56%.
Embodiment 29
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL isopropylcarbinol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), Scium trichloride (4.2mmol), Isosorbide-5-Nitrae-diazabicyclo [2.2.2] octane (4.2mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, camphorate sulfonic acid (42mmol) in hexanaphthene (500mL) solution of peroxidation dihydroartemisinic acid 3.Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 64g, three step total recoverys 53%.
Embodiment 30
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd (OH) 2/C (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), calcium chloride (424mmol), sodium bicarbonate (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 61g, three step total recoverys 51%.
Embodiment 31
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), Scium trinitrate (42mmol), potassium hydroxide (420mmol) join in 1000mL ether.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of peroxidation dihydroartemisinic acid 3, add Indian red (420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 71g, three step total recoverys 59%.
Embodiment 32
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL ethanol, 25 DEG C, in atmosphere of hydrogen (50bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (99g, 420mmol), lanthanum-cerium chloride (420mmol), Sulphaguanidine (420mmol) join in 1000mL Virahol.At-40 DEG C, in system, slowly drip Peracetic Acid (420mmol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in hexanaphthene (500mL) solution of peroxidation dihydroartemisinic acid 3, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 69g, three step total recoverys 57%.
Embodiment 33
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methyl alcohol, react 24 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Cerium II Chloride (424mmol), diisopropyl ethyl amine (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 10 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 59g, three step total recoverys 49%.
Embodiment 34
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL propyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), lanthanum fluoride (424mmol), Dicyanodiamide (4.2mol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in methyl-sulphoxide (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 58g, three step total recoverys 48%.
Embodiment 35
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methylene dichloride, react 12 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Lanthanum trichloride (424mmol), sodium hydroxide (424mmol) join in 1000mL dithiocarbonic anhydride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 69g, three step total recoverys 57%.
Embodiment 36
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (427mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), cerium oxide (424mmol), potassium hydroxide (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 66g, three step total recoverys 55%.
Embodiment 37
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (50bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), zirconium dioxide (424mmol), diisopropyl ethyl amine (424mmol) join in 1000mL ether.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 70g, three step total recoverys 58%.
Embodiment 38
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), lanthanum hexaborane (424mmol), cesium carbonate (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, camphorate sulfonic acid (4.2mol) in Virahol (500mL) solution of peroxidation dihydroartemisinic acid 3.Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 66g, three step total recoverys 55%.
Embodiment 39
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (427mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), Scium trinitrate (424mmol), sodium hydroxide (4.2mmol) join in 1000mL methyl-sulphoxide.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in DMF (500mL) solution of peroxidation dihydroartemisinic acid 3, add copper trifluoromethanesulfcomposite (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 71g, three step total recoverys 59%.
Embodiment 40
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL acetone, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of peroxidation dihydroartemisinic acid 3
Dihydroartemisinic acid (100g, 424mmol), ceric sulfate (424mmol), diisopropyl ethyl amine (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in toluene (500mL) solution of peroxidation dihydroartemisinic acid 3, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 57g, three step total recoverys 47%.
Embodiment 41
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (4.3mmol) join in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), triethylamine (420mmol) join in 1000mL methylene dichloride.In system, add methylsulfonyl chloride (420mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution, organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Scium trioxide (4.2mmol), salt of wormwood (4.2mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 67g, four step total recoverys 56%.
Embodiment 42
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (427mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), pyridine (6.4mol) join in 1000mL acetone.Add AcCl (424mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution, organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Scium trinitrate (424mmol), sodium hydroxide (4.2mmol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 65g, four step total recoverys 54%.
Embodiment 43
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL methylene dichloride.In system, add MOMCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, ceric sulfate (424mmol), diisopropyl ethyl amine (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 67g, three step total recoverys 56%.
Embodiment 44
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), Dicyanodiamide (420mmol) join in 1000mL tetracol phenixin.In system, add propargyl bromide (420mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Tungsten oxide 99.999 (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in hexanaphthene (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid sherwood oil recrystallization, obtains colourless acicular crystal 59g, four step total recoverys 49%.
Embodiment 45
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (43mmol) join in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (50bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), salt of wormwood (420mmol) join in 1000mL acetone, and add methyl iodide (420mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous magnesium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, sodium wolframate (4.2mmol), salt of wormwood (4.2mmol) join in 1000mL ethanol.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 72g, four step total recoverys 60%.
Embodiment 46
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (43mmol) join in 1000mL ethanol, (50bar) room temperature reaction 12 hours in atmosphere of hydrogen.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (6.4mol) join in 1000mL tetrahydrofuran (THF).In system, add methyl iodide (4.2mol) at 0 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, phospho-molybdic acid (42mmol), sodium hydroxide (420mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 70g, four step total recoverys 58%.
Embodiment 47
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (6.3mol) join in 1000mL methyl alcohol, and add allyl bromide 98 (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, sodium wolframate (424mmol), Sulphaguanidine (4.2mol) join in 1000mL n-propyl alcohol.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add aluminum chloride (42mmol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 48
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), diisopropylethylamine (12.7mol) join in 1000mL methylene dichloride.In system, add methylsulfonyl chloride (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Phosbloc cerium (424mmol), cesium carbonate (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 72g, four step total recoverys 60%.
Embodiment 49
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (4.3mmol) join in 1000mL methyl alcohol, 25 DEG C, in atmosphere of hydrogen (100bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), triethylamine (6.3mol) join in 1000mL tetrahydrofuran (THF).In system, add MOMCl (420mmol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, phospho-molybdic acid (4.2mmol), triethylamine (420mmol) join in 1000mL ethanol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 70g, four step total recoverys 58%.
Embodiment 50
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol) joins in 1000mL ether.In system, add methyl-chloroformate (420mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, clorox (4.2mmol), sodium hydroxide (4.2mmol) joins in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, camphorate sulfonic acid (42mmol) in hexanaphthene (500mL) solution of dihydroartemisinic acid derivative 5.Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 67g, four step total recoverys 56%.
Embodiment 51
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL ethanol, 25 DEG C, in atmosphere of hydrogen (50bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), diisopropylethylamine (6.3mol) join in 1000mL methylene dichloride.In system, add allyl bromide 98 (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum-cerium chloride (420mmol), salt of wormwood (420mmol) join in 1000mL Virahol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in hexanaphthene (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 71g, four step total recoverys 59%.
Embodiment 52
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (6.4mol) join in 1000mL tetrahydrofuran (THF).In system, add methyl iodide (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, clorox (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 64g, four step total recoverys 53%.
Embodiment 53
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (4.3mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 2 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), pyridine (4.2mol) join in 1000mL acetonitrile.In system, add methylsulfonyl chloride (12.7mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, cerous nitrate (424mmol), sodium hydroxide (4.2mol) join in 1000mLDMF.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in sherwood oil (500mL) solution of dihydroartemisinic acid derivative 5, add aluminum chloride (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 59g, four step total recoverys 49%.
Embodiment 54
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), cesium carbonate (6.3mol) join in 1000mL methylene dichloride.In system, add TBSCl (2.1mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum trioxide (42mmol), triethylamine (420mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 67g, four step total recoverys 56%.
Embodiment 55
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (4.3mmol) join in 1000mL methyl alcohol, 25 DEG C, in atmosphere of hydrogen (100bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), pyridine (6.3mol) join in 1000mL methylene dichloride, and in system, add THPCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, chromium trioxide (4.2mmol), potassium hydroxide (420mmol) join in 1000mL methyl alcohol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add iron trichloride (420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 63g, four step total recoverys 52%.
Embodiment 56
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), salt of wormwood (6.3mol) join in 1000mL acetone, and in system, add methyl iodide (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum nitrate (420mmol), sodium hydroxide (420mmol) join in 1000mL propyl alcohol.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, add copper trifluoromethanesulfcomposite (4.2mol) in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5.Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 57
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), salt of wormwood (420mol) join in 1000mL tetrahydrofuran (THF).In system, add Vinyl chloroformate (420mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Lanthanum trichloride (4.2mmol), sodium hydroxide (420mmol) join in 1000mL toluene.At 60 DEG C, in system, slowly drip the hydrogen peroxide (4.2mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 65g, four step total recoverys 54%.
Embodiment 58
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (50bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (6.4mol) join in 1000mL tetrahydrofuran (THF).In system, add methyl iodide (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, zirconium dioxide (424mmol), 1,8-diazabicyclo [5.4.0] 11 carbon-7-alkene (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of allyl group superoxide 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 73g, four step total recoverys 61%.
Embodiment 59
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL ether.In system, add TESCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 3
Compound 4, chromium chloride (424mmol), diisopropyl ethyl amine (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 73g, four step total recoverys 61%.
Embodiment 60
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (4.3mmol) join 1000mL1, in 4-dioxane ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), imidazoles (420mmol) join in 1000mL acetone.In system, add TsCl (420mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, zirconium oxychloride (4.2mmol), potassium hydroxide (4.2mmol) join in 1000mL ethyl acetate.At-78 DEG C, in system, slowly add peroxy tert-butyl alcohol (420mmol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (42mmol).Revolve after reaction carries out 6 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 61
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), sodium carbonate (12.7mol) join in 1000mL tetrahydrofuran (THF).In system, add BnCl (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Losantin (424mmol) join in 1000mL ethanol.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 10 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 71g, four step total recoverys 59%.
Embodiment 62
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), salt of wormwood (420mmol) join in 1000mL tetrahydrofuran (THF).In system, add chloroformic acid-2,2,2-trichloro ethyl ester (420mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum nitrate (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL methyl alcohol.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 63
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL methylene dichloride.In system, add PivCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum-cerium chloride (424mmol), tetramethyl guanidine (424mmol) joins in 1000mL benzene.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 58g, four step total recoverys 48%.
Embodiment 64
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), salt of wormwood (420mol) join in 1000mL tetrahydrofuran (THF).In system, add methyl iodide (420mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Lanthanum trichloride (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid, Cu/Dowex (42mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 65g, four step total recoverys 54%.
Embodiment 65
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL ethanol, 25 DEG C, in atmosphere of hydrogen (50bar) react 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), sodium bicarbonate (2.1mol) join in 1000mL methylene dichloride.In system, add Acetyl Chloride 98Min. (6.3mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, clorox (420mmol), salt of wormwood (420mmol) join in 1000mL Virahol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in hexanaphthene (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (42mmol).Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 60g, four step total recoverys 50%.
Embodiment 66
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Raney nickel (4.3mmol) join in 1000mL tetrahydrofuran (THF), and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), imidazoles (12.7mol) join in 1000mL tetrahydrofuran (THF), and in system, add THPCl (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, vanadium oxide (424mmol), pyridine (4.2mol) join in 1000mL dithiocarbonic anhydride.At 60 DEG C, in system, slowly add trifluoro Peracetic Acid (42mol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in sherwood oil (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 12 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 65g, four step total recoverys 54%.
Embodiment 67
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methyl alcohol, react 24 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (12.7mol) join in 1000mL acetone, and in system, add monobromethane (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum hydroxide (424mmol), sodium hydroxide (4.2mol) join in 25mL propyl carbinol.At 60 DEG C, in system, slowly add metachloroperbenzoic acid (42mol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid Isosorbide-5-Nitrae-dioxane recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 68
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), pyridine (12.6mol) join in 1000mL toluene.In system, add TBSCl (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, clorox (420mmol) join in 1000mL propyl alcohol.At-78 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid hexanaphthene recrystallization, obtains colourless acicular crystal 64g, four step total recoverys 53%.
Embodiment 69
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (427mmol) joins in 1000mL methyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 6 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), pyridine (6.4mol) join in 20000mL tetrahydrofuran (THF), and in system, add bromocyclohexane (4.2mol) at 0 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, clorox (424mmol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly add Peracetic Acid (4.2mol), reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add trifluoroacetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid Diethyl ether recrystallization, obtains colourless acicular crystal 66g, four step total recoverys 55%.
Embodiment 70
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL propyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL methylene dichloride.In system, add methylsulfonyl chloride (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum fluoride (424mmol), Isosorbide-5-Nitrae-diaza-bicyclo [2.2.2] octane (4.2mol) join in 20000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts, and merges organic phase anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 59g, four step total recoverys 49%.
Embodiment 71
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL methylene dichloride.In system, add N-PROPYLE BROMIDE (2.1mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, cerous hydroxide (42mmol), N, N, N ', N ' ,-Tetramethyl Ethylene Diamine (424mmol) joins in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 67g, four step total recoverys 56%.
Embodiment 72
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL toluene, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), pyridine (12.7mol) join in 1000mL acetonitrile, and in system, add TESCl (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Phosbloc (424mmol), diisopropyl ethyl amine (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 10 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 70g, four step total recoverys 58%.
Embodiment 73
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), Al 2o 3/ Rh (4.3mmol) joins in 1000mL methyl alcohol ,-50 DEG C, in atmosphere of hydrogen (1bar) react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), cesium carbonate (420mmol) join in 1000mL acetone.In system, add BzCl (420mmol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Scium trichloride (4.2mmol), sodium hydroxide (4.2mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, camphorate sulfonic acid (42mmol) in hexanaphthene (500mL) solution of dihydroartemisinic acid derivative 5.Revolve after reaction carries out 4 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solids with methanol recrystallization, obtains colourless acicular crystal 70g, four step total recoverys 58%.
Embodiment 74
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), nickelous chloride (43mmol), sodium borohydride (427mmol) join in 1000mL toluene, room temperature reaction 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (99g, 98%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol) joins in 1000mL acetone.In system, add diazomethane (2.1mol) at 0 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum hydroxide (42mmol), potassium hydroxide (420mmol) join in 1000mL ethanol.At-40 DEG C, in system, slowly drip the hydrogen peroxide (420mmol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add Cu (Tc) 2(420mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 75
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methyl alcohol, react 24 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), diisopropylethylamine (12.7mol) join in 1000mL methyl alcohol.In system, add MOMCl (4.2mol) at 60 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, sodium perchlorate (424mmol), diisopropyl ethyl amine (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetone (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with ethyl acetate recrystallization, obtains colourless acicular crystal 69g, four step total recoverys 57%.
Embodiment 76
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (427mmol) join in 1000mL Virahol, and in 25 DEG C of atmosphere of hydrogen, (1bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), pyridine (6.3mol) join in 1000mL acetone.In system, add methylsulfonyl chloride (4.2mmol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, potassium bichromate (424mmol), pyridine (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add acetic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 70g, four step total recoverys 58%.
Embodiment 77
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL methyl alcohol, react 12 hours, add a small amount of shrend and to go out reaction.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), imidazoles (6.4mol) join in 1000mL tetrahydrofuran (THF).In system, add TBSCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Lanthanum trichloride (424mmol), sodium hydroxide (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 60g, four step total recoverys 50%.
Embodiment 78
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), platinum oxide (427mmol) join in 1000mL propyl alcohol, and in 60 DEG C of atmosphere of hydrogen, (100bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (99g, 420mmol), lithium hydroxide (420mmol) join in 1000mLDMF.-50 DEG C in system under add TMSCl (420mmol), reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, cerous hydroxide (424mmol), sodium carbonate (4.2mol) join in 1000mL methylene dichloride.At-78 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 63g, four step total recoverys 52%.
Embodiment 79
(1) synthesis of dihydroartemisinic acid 2
Arteannuinic acid (100g, 427mmol), 10%Pd/C (43mmol) join in 1000mL ethanol, and in room temperature, atmosphere of hydrogen, (50bar) reacts 12 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (2.1mol) join in 1000mL acetone.In system, add monobromethane (6.3mol) at 0 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Lanthanum trichloride (42mmol), sodium hydroxide (420mmol) join in 1000mL acetonitrile.At-40 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 50%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-40 DEG C, under oxygen existent condition, in methylene dichloride (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (424mmol).Revolve after reaction carries out 3 hours and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid with methylene chloride recrystallization, obtains colourless acicular crystal 57g, four step total recoverys 47%.
Embodiment 80
(1) synthesis of dihydroartemisinic acid 2
At-50 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (427mmol), sodium borohydride (427mmol) join in 1000mL methyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), salt of wormwood (12.7mol) join in 1000mL acetone, and in system, add methyl iodide (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, Lanthanum trichloride (424mmol), potassium hydroxide (4.2mol) join in 1000mL acetonitrile.At 60 DEG C, in system, slowly drip the hydrogen peroxide (42mol) of 70%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
60 DEG C, under oxygen existent condition, in acetonitrile (500mL) solution of dihydroartemisinic acid derivative 5, add tosic acid (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid acetone recrystallization, obtains colourless acicular crystal 65g, four step total recoverys 54%.
Embodiment 81
(1) synthesis of dihydroartemisinic acid 2
At 60 DEG C, arteannuinic acid (100g, 427mmol), nickelous chloride (4.3mol), sodium borohydride (8.5mol) join in 1000mL propyl alcohol, react 24 hours.Reaction mixture, through diatomite filtration, revolves and steams removing organic solvent, obtain white solid (100g, 99%).
(2) synthesis of dihydroartemisinic acid derivative 4
Dihydroartemisinic acid (100g, 424mmol), triethylamine (6.4mol) join in 1000mL methylene dichloride.In system, add MsCl (4.2mol) at-50 DEG C, reaction is spent the night.In reaction solution, add a small amount of water, revolve and steam removing organic solvent, ethyl acetate (1000mL) dilute reaction solution.Organic phase washed with water (100mL × 3), anhydrous sodium sulfate drying, suction filtration, revolves and steams except desolventizing, and product directly drops into next step reaction.
(3) synthesis of peroxidation dihydroartemisinic acid derivative 5
Compound 4, lanthanum hexaborane (424mmol), cesium carbonate (424mmol) join in 1000mL acetonitrile.At-78 DEG C, in system, slowly drip the hydrogen peroxide (4.2mol) of 30%, reaction is spent the night.Revolve and steam removing organic solvent, residual phase ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing, product directly drops into next step reaction.
(4) synthesis of Artemisinin 1
-78 DEG C, under oxygen existent condition, in Virahol (500mL) solution of dihydroartemisinic acid derivative 5, add copper trifluoromethanesulfcomposite (4.2mol).Revolve after reaction carries out 1 hour and steam removing organic solvent, residue with ethyl acetate (500mL × 3) extracts.Merge organic phase anhydrous sodium sulfate drying, suction filtration, revolve and steam except desolventizing obtains faint yellow solid.This solid normal hexane recrystallization, obtains colourless acicular crystal 72g, four step total recoverys 60%.
Artemisinin: 1hNMR (400MHz, CDCl 3) δ 5.83 (s, 1H), 3.36 (brdq, J=7.2,5.5Hz, 1H), 2.40 (brddd, J=14.8,13.8,3.9Hz, 1H), 2.06-1.93 (m, 2H), 1.90-1.82 (m, 1H), 1.78-1.67 (m, 2H), 1.50-1.30 (m, 3H), 1.41 (s, 3H), (1.17 d, J=7.3Hz, 3H), 1.09-1.00 (m, 2H), 0.97 (d, J=5.7Hz, 3H); 13cNMR (100MHz, CDCl 3) δ 171.9,105.3,93.6,79.4,49.9,44.8,37.4,35.8,33.5,32.8,25.1,24.7,23.3,19.7,12.4.
Although content of the present invention has done detailed introduction by above preferred embodiment, will be appreciated that above-mentioned description should not be considered to limitation of the present invention.After those skilled in the art have read foregoing, for multiple amendment of the present invention and substitute will be all apparent.Therefore, protection scope of the present invention should be limited to the appended claims.

Claims (26)

1. a synthetic method for medicinal artemisinin, is characterized in that, described method comprises the steps:
Step one: take arteannuinic acid as starting raw material, generates dihydroartemisinic acid 2 through reduction reaction;
Step 2: dihydroartemisinic acid 2 is by obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl;
In step 2, described refers under alkalescence exists to carboxy protective, dihydroartemisinic acid 2 is in organic solvent through obtaining dihydroartemisinic acid derivative 4 to the protection of carboxyl, wherein: dihydroartemisinic acid 2 is 1:(1 ~ 30 with the consumption mol ratio of alkali), temperature of reaction is-50 ~ 60 DEG C, and described alkali is mineral alkali or organic bases; Described consumption of organic solvent is 100 ~ 5000mL/ mole;
Step 3: dihydroartemisinic acid derivative 4 obtains corresponding peroxidation dihydroartemisinic acid derivative 5 through peroxidation again;
In step 3, described oxidizing reaction refers under alkali and metal catalyst exist, in organic solvent, obtain corresponding peroxidation dihydroartemisinic acid derivative with peroxide oxidation dihydroartemisinic acid derivative 4;
The metal catalyst of described oxidizing reaction is calcium, sodium, molybdenum, chromium, lanthanum, cerium, tungsten, scandium, titanium, zirconium, the salt of vanadium and oxide compound, described calcium, sodium, molybdenum, chromium, lanthanum, cerium, tungsten, scandium, titanium, zirconium, the salt of vanadium and oxide compound are phospho-molybdic acid, chromium trioxide, chromium chloride, potassium bichromate, calcium chloride, Losantin, Tungsten oxide 99.999, sodium wolframate, Scium trioxide, Scium trinitrate, Scium trichloride, zirconium dioxide, zirconium oxychloride, vanadium oxide, vanadic acid sodium, cerous nitrate, ceric sulfate, cerium oxide, Cerium II Chloride, cerous hydroxide, lanthanum-cerium chloride, Phosbloc cerium, lanthanum trioxide, Lanthanum trichloride, lanthanum hydroxide, lanthanum nitrate, Phosbloc, lanthanum fluoride, lanthanum hexaborane, clorox or sodium perchlorate,
The mol ratio of described metal catalyst and dihydroartemisinic acid derivative 4 is 1:1 ~ 100;
Described dihydroartemisinic acid derivative 4 is 1:1 ~ 100 with the mol ratio of superoxide used;
Step 4: peroxidation dihydroartemisinic acid derivative 5 is reset under acid catalysis, repurity obtains Artemisinin 1;
The route map of above-mentioned steps is specific as follows:
R-in described dihydroartemisinic acid derivative 4 is the group for the protection of acidic group.
2. the synthetic method of medicinal artemisinin according to claim 1, it is characterized in that: in step one, described reduction reaction refers to that arteannuinic acid is under reaction solvent exists, with be carried on the palladium of charcoal or palladium hydroxide, the rhodium being carried on aluminium sesquioxide, Raney nickel, platinum oxide one of them for catalyzer, be reductive agent with hydrogen, or be reductive agent with sodium borohydride under the existence of nickelous chloride, wherein the mol ratio of arteannuinic acid and described catalyzer is 1:0.01 ~ 1, and the mol ratio of arteannuinic acid and nickelous chloride, sodium borohydride is 1:0.01 ~ 10:1 ~ 20.
3. the synthetic method of medicinal artemisinin according to claim 2, is characterized in that: in step one, and when taking hydrogen as reductive agent, the pressure reacting hydrogen used is 1 ~ 100bar, and temperature is-50 ~ 60 DEG C.
4. the synthetic method of medicinal artemisinin according to claim 3, is characterized in that: in step one, and the pressure of described reduction reaction hydrogen used is 50bar, and temperature of reaction is 25 DEG C.
5. the synthetic method of medicinal artemisinin according to claim 2, is characterized in that: in step one, and when described is reductive agent with sodium borohydride under the existence of nickelous chloride, reduction reaction temperature is-50 ~ 60 DEG C.
6. the synthetic method of medicinal artemisinin according to claim 5, is characterized in that: described reduction reaction temperature is-40 DEG C.
7. the synthetic method of medicinal artemisinin according to claim 2, is characterized in that: described reaction solvent is methyl alcohol, ethanol, propyl alcohol, Virahol, propyl carbinol, isopropylcarbinol, tetrahydrofuran (THF) or toluene.
8. the synthetic method of medicinal artemisinin according to claim 1, is characterized in that: in step 2, and alkali used is cesium carbonate, salt of wormwood, sodium carbonate, sodium bicarbonate, saleratus, triethylamine, diisopropylethylamine, pyridine or imidazoles.
9. the synthetic method of medicinal artemisinin according to claim 1, it is characterized in that: in step 2, described organic solvent is tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, tetracol phenixin, Virahol, DMF or DMSO.
10. the synthetic method of medicinal artemisinin according to claim 1, it is characterized in that: in step 2, described to carboxy protective, protection reagent used is methyl iodide, diazomethane, methoxymethyl chlorine, methyl-chloroformate, Vinyl chloroformate, chloroformic acid-2, 2, 2-trichloro ethyl ester, trimethyl silicon based chlorine, the chloro-tetrahydropyrans of 2-, Acetyl Chloride 98Min., methylsulfonyl chloride, Tosyl chloride, benzyl chloride, bromotoluene, valeryl chlorine, the silica-based chlorine of triethyl, t-Butyldimethylsilyl chlorine or the silica-based chlorine of tert-butyl diphenyl, dihydroartemisinic acid is 1:1 ~ 10 with the mole dosage ratio of protection reagent.
The synthetic method of 11. medicinal artemisinin according to claim 1, is characterized in that: the R-in described dihydroartemisinic acid derivative 4 is alkyl, thiazolinyl, alkynyl, aryl, cycloalkyl group, MOM, TMS, THP, Ac, Ms, Ts, Bz, Piv, TES, TBS or TBDPS.
The synthetic method of 12. medicinal artemisinin according to claim 11, is characterized in that: described alkyl refers to have C nh 2n+1general structure, the aliphatic group of straight or branched, n=1 ~ 8;
Described thiazolinyl refers to the alkyl of the straight or branched containing one or more carbon-carbon double bond, containing 2-8 carbon atom;
Described alkynyl refers to the alkyl of the straight or branched containing one or more carbon-carbon triple bond, containing 2-8 carbon atom;
Described aryl refers to phenyl, naphthyl, anthryl, phenanthryl, dibiphenylyl, terphenyl, trityl group, phenmethyl, 2-menaphthyl, 9-anthracene ethyl, 9-luxuriant and rich with fragrance methyl, 3-diphenyl ethyl, pyrryl, furyl, thienyl, pyridyl, benzofuryl, benzothienyl, indyl, quinolyl or isoquinolyl;
Described cycloalkyl group is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, suberyl, two cyclic terpene bases, cyclobutene base, cyclopropenyl radical, cyclopentenyl or cyclohexenyl.
The synthetic method of 13. medicinal artemisinin according to claim 12, it is characterized in that: described alkyl refers to: methyl, ethyl, propyl group, sec.-propyl, 2-methyl isophthalic acid-propyl group, 2-methyl-2-propyl, 2-methyl-1-butene base, 3-methyl isophthalic acid-butyl, 2-methyl-3-butyl, 2, 2-dimethyl-1-butyl, 2-methyl-1-pentene base, 3-methyl-1-pentene base, 4-methyl-1-pentene base, 2-methyl-2 amyl group, 3-methyl-2-amyl group, 4-methyl-2-amyl group, 2, 2-dimethyl-1-butyl, 3, 3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl, amyl group, hexyl, heptyl or octyl group,
Described thiazolinyl refers to: vinyl, propenyl, butenyl, pentenyl, hexenyl, butadienyl, piperylene base, oneself two thiazolinyls or 2-ethyl hexyl thiazolinyl;
Described alkynyl refers to: ethynyl, proyl, butynyl, pentynyl, hexin base, valerylene base or 5-methyl-2-heptyne base.
The synthetic method of 14. medicinal artemisinin according to claim 1, is characterized in that: in step 3, the organic solvent of described oxidizing reaction, and its consumption is 50 ~ 10000mL/ mole, and temperature of reaction is-78 ~ 60 DEG C.
The synthetic method of 15. medicinal artemisinin according to claim 14, it is characterized in that: in step 3, the organic solvent of described oxidizing reaction is acetone, tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, Virahol, DMF, DMSO or benzene.
The synthetic method of 16. medicinal artemisinin according to any one of claim 1-15, is characterized in that: in step 3, and described dihydroartemisinic acid derivative 4 is 1:(1 ~ 100 with the mol ratio of superoxide used).
The synthetic method of 17. medicinal artemisinin according to claim 16, is characterized in that: in step 3, and the superoxide of described oxidizing reaction is metachloroperbenzoic acid, hydrogen peroxide, peroxy tert-butyl alcohol, Peracetic Acid or peroxy trifluoroacetic acid.
The synthetic method of 18. medicinal artemisinin according to claim 17, is characterized in that: described hydrogen peroxide is the aqueous hydrogen peroxide solution of 30%, 50% or 70%.
The synthetic method of 19. medicinal artemisinin according to any one of claim 1-15, is characterized in that: in step 3, and described dihydroartemisinic acid derivative 4 is 1:(0.01 ~ 10 with the mol ratio of alkali).
The synthetic method of 20. medicinal artemisinin according to claim 19, it is characterized in that: described alkali is cesium carbonate, salt of wormwood, sodium carbonate, sodium bicarbonate, saleratus, sodium hydroxide, potassium hydroxide, lithium hydroxide, triethylamine, diisopropylethylamine, pyridine, imidazoles, 1,8-diazabicyclo [5.4.0] 11 carbon-7-alkene, 1,4-diazabicyclo [2.2.2] octane, Dicyanodiamide, tetramethyl guanidine, Sulphaguanidine or N, N, N', N'-Tetramethyl Ethylene Diamine.
The synthetic method of 21. medicinal artemisinin according to claim 1, it is characterized in that: in step 4, described acid catalyzed rearrangement reaction refers to that peroxidation dihydroartemisinic acid derivative 5 obtains Artemisinin 1 through acid catalyzed rearrangement in organic solvent and under oxygen atmosphere; Described temperature of reaction is-78 ~ 60 DEG C.
The synthetic method of 22. medicinal artemisinin according to claim 21, is characterized in that: described solvent load is 50 ~ 10000mL/ mole.
The synthetic method of 23. medicinal artemisinin according to claim 22, is characterized in that: described solvent is acetone, tetrahydrofuran (THF), ether, methylene dichloride, chloroform, acetonitrile, toluene, methyl alcohol, ethanol, Virahol, sherwood oil, hexanaphthene, normal hexane, DMF, DMSO, n-propyl alcohol, propyl carbinol, ethyl acetate or benzene.
The synthetic method of 24. medicinal artemisinin according to claim 21, is characterized in that: described acid is that Bronsted acid or Lewis are sour; The mol ratio of acid used and peroxidation dihydroartemisinic acid derivative 5 is 1:(1 ~ 100).
The synthetic method of 25. medicinal artemisinin according to claim 24, is characterized in that: described acid is p-methyl benzenesulfonic acid, trifluoroacetic acid, acetic acid, camphorsulfonic acid, copper trifluoromethanesulfcomposite, aluminum chloride, iron trichloride, cupric chloride, cupric oxide, ferric oxide, Cu/Dowex resin or thiophene-2-carboxylic acid copper.
The synthetic method of 26. medicinal artemisinin according to claim 1, is characterized in that: described purification process organic or inorganic solvent carries out column chromatography or recrystallization.
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CN103087074A (en) * 2012-12-14 2013-05-08 湖南科源生物制品有限公司 Method of semi-synthesizing artemisinin
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