CN1434033A - 2,5-dimethoxy-4-ethyl phenethyl amine sulfide hydrochloride and preparation process and use thereof - Google Patents
2,5-dimethoxy-4-ethyl phenethyl amine sulfide hydrochloride and preparation process and use thereof Download PDFInfo
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- CN1434033A CN1434033A CN 03118591 CN03118591A CN1434033A CN 1434033 A CN1434033 A CN 1434033A CN 03118591 CN03118591 CN 03118591 CN 03118591 A CN03118591 A CN 03118591A CN 1434033 A CN1434033 A CN 1434033A
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Abstract
The present invention relates to 2,5-dimethoxy-4-ethylthiophenethylamine hydrochloride and its preparation method. Said invention provides its structure formula and its adopted steps: under the acidic condition using zinc powder to make the 2,5-dimethoxybenzenesulfonyl chloride undergo the processes of reduction reaction, reduced pressure distillation, and condensation reaction with bromoethane under the alkaline condition, and reduced pressure distillation to obtain yellow oil liquid 2,5-dimethoxyethyl phenyl sulide, making it react with phosphorus oxychloride and dimethyl formamide, and making the obtained product and nitromethane produce condensation, using lithium alumium hydride reduction in furanidine and using hydrochloric acid to make acidification so as to obtain the invented end product 2.5-dimethoxy-4-ethylthio-phenetylamine
Description
Technical field
The present invention relates to a kind of 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride and method for making and purposes.
Background technology
As a kind of new compound, 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride and synthetic method thereof are not seen bibliographical information as yet.
Summary of the invention
Task of the present invention provides a kind of new compound 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride and method for making and purposes.
Technical scheme provided by the invention is: 2, and 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride, its structural formula is
The present invention also provides the method for making of above-claimed cpd, under 70~80 ℃, acidic conditions (pH<1), 2,5-dimethoxy benzene sulfonyl chloride is through zinc powder reduction, and underpressure distillation then obtains 2,5-dimethoxy thiophenol, gained 2,5-dimethoxy thiophenol are at 70~80 ℃, alkaline condition (pH>10) down and the monobromethane condensation, get yellow oily liquid 2 through underpressure distillation, 5-dimethoxy ethyl phenyl sulfide; 2,5-dimethoxy ethyl phenyl sulfide and phosphorus oxychloride and dimethyl formamide react under 70~80 ℃ of conditions and obtain white solid 2,5-dimethoxy-4 '-ethyl phenyl sulfide formaldehyde, products therefrom obtains red solid 2 with the Nitromethane 99Min. condensation again, 5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene, with 2,5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene in tetrahydrofuran (THF) with lithium aluminium hydride reduce 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine, 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine obtains final product 2 with hcl acidifying, 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride.
2,5-dimethoxy benzene sulfonyl chloride can make by following method, and ethylene dichloride and terephthaldehyde's ether are mixed stirring and dissolving, be cooled to 0~10 ℃ of following agitation and dropping chlorsulfonic acid and sulfur oxychloride, tell lower floor's oil reservoir, to its distill yellow solid 2,5-dimethoxy benzene sulfonyl chloride.
The present invention also provides and has been used to prepare 2, the intermediate 2 of 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride, and 5-dimethoxy-4 '-ethyl phenyl sulfide ethamine, its structural formula is:
2 of the present invention's preparation, 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride can be used as the intermediate of medicine, especially for the pharmaceutical intermediate of treatment nervous system disease.
Embodiment
In the 250ml there-necked flask, add 105ml ethylene dichloride, 13.5g terephthaldehyde ether, stirring and dissolving, ice bath cooling (0~10 ℃), stir and drip 26.5ml chlorsulfonic acid and 10ml sulfur oxychloride down, reacted 2 hours, and with in its impouring 280ml frozen water, told lower floor's oil reservoir under stirring, steam and remove methylene dichloride (recovery), get yellow solid 2,5-dimethoxy benzene sulfonyl chloride, oven-dried weight 19.8g, productive rate 85%, fusing point 115-117 ℃.
In the 500ml there-necked flask, add the 68ml water and the 23ml vitriol oil, when treating that temperature drops to about 70 ℃, adding 12g2,5-dimethoxy benzene sulfonyl chloride and 18g zinc powder reacted 1 hour down at 80 ℃, and filtration, decompression, steaming are slipped and are obtained 8.2g2,5-dimethoxy thiophenol.
In three mouthfuls of hydrochloric acid bottles of 250ml, add 3g potassium hydroxide and 50ml dehydrated alcohol, stirring and dissolving adds 8g2, and 5-dimethoxy thiophenol is dissolved in the solution of 20ml dehydrated alcohol, drip the 9g monobromethane again, reflux 1.5h boils off ethanol, uses twice of 40ml dichloromethane extraction, steam except that behind the methylene dichloride, underpressure distillation gets light yellow oily liquid 2,5-dimethoxy ethyl phenyl sulfide 8.2g, productive rate 80%.
Under the ice bath cooling, the 9.7ml phosphorus oxychloride is joined in the 100ml there-necked flask, drip the 11.5ml dimethyl formamide, drip 8g2 again, 5-dimethoxy ethyl phenyl sulfide, 75 ℃ of stirring reactions 1 hour, placement is spent the night, suction filtration gets light yellow solid (is white solid through the Virahol recrystallization) 8.8g, and this compound is 2,5-dimethoxy-4 '-Z sulfenyl phenyl aldehyde.
Add 8g2 in the 100ml there-necked flask, 5-dimethoxy-4 '-ethyl phenyl sulfide formaldehyde, 20ml Nitromethane 99Min. add 0.5g anhydrous acetic acid ammonium after the heating for dissolving, backflow 1.5h, separate out red solid 2 after the cooling, 5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene 8.5g, productive rate 78.2%.
Under the ice bath cooling, in the 500ml there-necked flask, add 210ml anhydrous tetrahydro furan, 8g lithium aluminium hydride, slowly add 8g2,5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene, backflow 7h, add 40ml Virahol, 15 milliliter 5% sodium hydroxide successively, filter, steam desolventize, underpressure distillation obtains 5g 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine.With 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine is dissolved in 30ml ether and the 30ml Virahol, slowly drips dense 10ml, separates out white solid, filtration, dry 5.5 grams 2 that get, and 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride is analyzed content 〉=98% through HPLC.
Claims (6)
2. 2, the method for making of 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride, it is characterized in that: under 70~80 ℃, acidic conditions, 2,5-dimethoxy benzene sulfonyl chloride is through zinc powder reduction, underpressure distillation then, obtain 2,5-dimethoxy thiophenol, gained 2,5-dimethoxy thiophenol under 70~80 ℃, alkaline condition with the monobromethane condensation, get 2 through underpressure distillation, 5-dimethoxy ethyl phenyl sulfide; 2,5-dimethoxy ethyl phenyl sulfide and phosphorus oxychloride and dimethyl formamide react under 70~80 ℃ of conditions and obtain 2,5-dimethoxy-4 '-ethyl phenyl sulfide formaldehyde, gained 2,5-dimethoxy-4 '-ethyl phenyl sulfide formaldehyde obtains 2 with the Nitromethane 99Min. condensation again, 5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene, with 2,5-dimethoxy-4 '-ethylmercapto group-beta-nitrostyrene in tetrahydrofuran (THF) with lithium aluminium hydride reduce 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine, 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethamine obtains final product 2,5 dimethoxy-4 's-ethyl phenyl sulfide ethylamine hydrochloride with hcl acidifying.
3. method for making according to claim 2, it is characterized in that: 2,5-dimethoxy benzene sulfonyl chloride makes by following method, ethylene dichloride and terephthaldehyde's ether are mixed stirring and dissolving, be cooled to 0~10 ℃ of following agitation and dropping chlorsulfonic acid and sulfur oxychloride, tell lower floor's oil reservoir, to its distill 2,5-dimethoxy benzene sulfonyl chloride.
5. 2,5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride is as the intermediate of preparation medicine.
6. the described purposes of claim 5 is characterized in that: 2, and 5-dimethoxy-4 '-ethyl phenyl sulfide ethylamine hydrochloride is as the pharmaceutical intermediate of treatment nervous system disease.
Priority Applications (1)
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CNB031185916A CN1193012C (en) | 2003-02-14 | 2003-02-14 | 2,5-dimethoxy-4-ethyl phenethyl amine sulfide hydrochloride and preparation process and use thereof |
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CNB031185916A CN1193012C (en) | 2003-02-14 | 2003-02-14 | 2,5-dimethoxy-4-ethyl phenethyl amine sulfide hydrochloride and preparation process and use thereof |
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CN1434033A true CN1434033A (en) | 2003-08-06 |
CN1193012C CN1193012C (en) | 2005-03-16 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101311162B (en) * | 2008-05-26 | 2010-04-14 | 浙江金伯士药业有限公司 | Method for preparing 2,5-dimethoxy phenylethylamine |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101311162B (en) * | 2008-05-26 | 2010-04-14 | 浙江金伯士药业有限公司 | Method for preparing 2,5-dimethoxy phenylethylamine |
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