CN109867734A - The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification - Google Patents
The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification Download PDFInfo
- Publication number
- CN109867734A CN109867734A CN201711266309.5A CN201711266309A CN109867734A CN 109867734 A CN109867734 A CN 109867734A CN 201711266309 A CN201711266309 A CN 201711266309A CN 109867734 A CN109867734 A CN 109867734A
- Authority
- CN
- China
- Prior art keywords
- cyclodextrin
- beta
- caffeic acid
- amido
- solvent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
The invention belongs to field of pharmaceutical chemistry research, and in particular to a kind of caffeic acid-amido-beta-cyclodextrin derivative (I) and preparation method thereof.The beta-cyclodextrin derivative (I) of the antioxidant caffeic acid modification has no document report.The present invention is with beta-cyclodextrin (β-CD) for raw material; it is reacted in a solvent in the presence of alkali with paratoluensulfonyl chloride; obtain mono- 6- deoxidation -6- p-toluenesulfonyl-beta-cyclodextrin (1); the product further reacts to obtain amine group-beta-cyclodextrin (2) with amine reagent, and compound (2) further reacts to obtain caffeic acid-amido-beta-cyclodextrin derivative (I) with caffeic acid；Caffeinic introducing assigns cyclodextrin certain antioxygenic property.
Description
Technical field
The present invention relates to a kind of caffeic acid modification cyclodextrin derivatives and preparation method thereof.
Background technique
Cyclodextrin be it is a kind of can be from the low oligosaccharide of ring-type of starch, in view of its special molecular structure and hydrophobic interior
Chamber effectively can form inclusion system by host-guest interaction with guest molecule, this feature makes cyclodextrin can be with
It is participated in the constructing of the supramolecular system based on cyclodextrin with number of ways.Constructing successful supramolecular system can be applied
In many related fieldss such as environmental protection and pharmacy.Cyclodextrin can by with guest pharmaceutical molecule forming bag mixture or chemical bond
The mode of object is connect to improve the physicochemical property of guest pharmaceutical, the water solubility of guest pharmaceutical is effectively improved, improves guest pharmaceutical
Stability and the bioavilability for promoting drug.In addition to this, folic acid, half can also be introduced in cyclodextrin supramolecular system
The targeting ligands such as lactose and hyaluronic acid and construct the pharmaceutical carrier with targeting property, and then for the targets of the diseases such as cancer
To treatment ".In view of cyclodextrin and its good aqueous solubility having, safety and low toxicity and the disimmune of derivative, cyclodextrin packet
Conjunction technology is increasingly extensive in the practical application of pharmaceutical field.
Caffeic acid and its ester have stronger antibacterial activity, antiviral activity, antioxidant activity and antitumor action, pharmacology
It is active very extensive, it is the hot spot compound of new drug development in recent years, medically has broad application prospects.
There is antioxidative cyclodextrin supramolecular system in order to obtain, construct the pharmaceutical carrier with antioxidant properties,
And then the guest pharmaceutical molecule forming bag mixture for being easy to oxidation deterioration, improve the physicochemical property of guest pharmaceutical, a kind of and coffee
The cyclodextrine derivatives of coffee acid coupling are designed and synthesize.
What this field needed to obtain brand new at present has certain antioxidative cyclodextrin supramolecular system, overcomes existing
Some deficiencies enrich the structure type of cyclodextrin supramolecular system, are applied to pharmaceutical field as pharmaceutical carrier.
Summary of the invention
The purpose of the present invention is overcoming deficiency in the prior art, the cyclodextrin for providing kind antioxidant caffeic acid modification is super
Molecular system (I) and preparation method thereof.The caffeic acid-amine group-beta-cyclodextrin (I) has no document report.
A kind of caffeic acid-amido-beta-cyclodextrin derivative (I) structure is as follows:
Wherein, the n indicates 0~10；
The present invention provides the caffeic acid of one kind as shown in formula (I)-amido-beta-cyclodextrin derivative (I) preparation method,
Synthetic route is shown below, comprising the following steps:
A) the compound β-CD reacts in a solvent in the presence of alkali with paratoluensulfonyl chloride, obtains mono- 6- deoxidation-
6- p-toluenesulfonyl-beta-cyclodextrin (1)；Wherein, β-CD and paratoluensulfonyl chloride, the molar ratio of alkali is 1: 2~2.2: 0.1~
0.2: 0.05~0.1, the reaction time is 2~6h, and reaction temperature is room temperature to 100 DEG C；
Solvent used is DMF or water or tetrahydrofuran or the common solvents such as ethyl acetate or acetone, and preferably water is as molten
Agent；
Alkali used is organic base such as pyridine, triethylamine, DBU etc., preferably triethylamine；Or be inorganic base such as NaOH etc.,
It is preferred that NaOH；
B) compound (1) carries out amido substitution reaction in organic solvent and generates mono- 6- deoxidation-amido-β-ring paste
Compounds (2)；Wherein, the reaction time be 6~for 24 hours, reaction temperature be room temperature to 70~100 DEG C；
Solvent used is tetrahydrofuran or alkyl halide or methanol (ethyl alcohol) or ethylenediamine, diethylenetriamine, preferably second two
The amine solvents such as amine；
C) compound (2) is reacted under the action of condensing agent with caffeic acid in organic solvent generates caffeic acid-amine
Group-beta-cyclodextrin derivative (I)；Wherein, the reaction time be 2~for 24 hours, reaction temperature be room temperature to 40 DEG C；
Organic solvent used is tetrahydrofuran or alkyl halide or DMF, preferably DMF etc.；
Condensing agent used is DCC or EDCHCl/NHS etc.；
The present invention reacts in a solvent using β-CD as raw material with paratoluensulfonyl chloride and alkali, obtains mono- (- 6- pairs of 6- deoxidation
Tosyl)-beta-cyclodextrin (1), which further reacts to obtain amine group-beta-cyclodextrin (2), the chemical combination with amine reagent
Object further reacts to obtain caffeic acid-amido-beta-cyclodextrin derivative (I) with caffeic acid；Caffeinic introducing assigns cyclodextrin
Certain antioxygenic property.
Specific embodiment
For a further understanding of the present invention, the preferred embodiment of the invention is described below with reference to embodiment, still
It should be appreciated that these descriptions are only further explanation the features and advantages of the present invention, rather than to the claims in the present invention
Limitation.The specific synthetic route of embodiment is as follows:
Embodiment 1
The synthesis of mono- 6- deoxidation -6- p-toluenesulfonyl-beta-cyclodextrin (1)
Mono- 6- deoxidation -6- p-toluenesulfonyl-beta-cyclodextrin (1), precise beta-cyclodextrin are synthesized using Aqueous phase
It (10.5g) and is slowly dissolve into the three-necked flask equipped with distilled water (65ml), after solution is sufficiently stirred at room temperature
Become white " milky " liquid, (0.86 gram of oxygen sodium hydroxide solution, is dissolved in 2.5 then to oxygen sodium hydroxide solution is slowly instilled in reaction solution
In milliliter distilled water), continue to be stirred at room temperature to solution and clarify；Precise paratoluensulfonyl chloride (1.3 grams) is dissolved in second
In nitrile (4 milliliters) solution, continues stirring to reaction at room temperature and complete；Filtering, the slow adjusting reaction solution of hydrochloric acid (2M)
PH value is had a large amount of white precipitate and generated at this time to 7.5, is filtered in a moment continuing stirring and is collected precipitating.Precipitating is tied again
Three times, net product, yield 10% can be obtained in vacuum drying to crystalline substance.1H NMR(CDCl3, 300MHz): δH, ppm 6.70 (d, 4H, J
=2.4), 4.38 (t, 1H), 4.12 (q, 2H), 3.41 (t, 2H), 1.92 (m, 2H), 1.56 (m, 2H), 1.30 (m, 5H)；
Embodiment 2
The synthesis of mono- 6- deoxidation-ethylenediamine-beta-cyclodextrin (2)
The mono- 6- deoxidation -6- p-toluenesulfonyl of precise-beta-cyclodextrin (1) is dissolved in the ethylenediamine through being dried,
It is stirred to react reaction solution under 60 degree 8 hours, reaction process is needed in N2Under the conditions of.It boils off after the completion of reaction most of molten
Agent instills residual reaction liquid in the acetone under stirring dropwise, generates white precipitate.It collects white precipitate and adds a small amount of water
Dissolution, aqueous solution is equally slowly dropped into the acetone under stirring, is collected precipitating and is obtained purer product.Repeat above-mentioned behaviour
Make, until TLC method confirmation product can be used only with mono- 6- deoxidation-ethylenediamine beta-cyclodextrin (2), yield 80%)；1H
NMR(CDCl3, 300MHz):1H NMR(CDCl3, 300MHz): δH, ppm 6.70 (d, 4H, J=2.4), 4.38 (t, 1H),
3.88 (d, 2H), 3.41 (t, 2H), 2.22 (s, 1H), 1.56 (m, 4H), 1.29 (m, 2H)；
Embodiment 3
The synthesis of caffeic acid-ethylenediamine group-beta-cyclodextrin derivative (II)
It weighs caffeic acid (0.45mmol) to be dissolved in 15mL DMF, n-hydroxysuccinimide (NHS) then is added
(0.06g) and DCC (0.11g) make reaction solution be protected from light stirring three hours at room temperature in N2 protection, wherein the NHS and DCC that are added
It is 1.2 equivalents relative to caffeic acid, is stirred at room temperature three hours, mono- 6- deoxidation-ethylenediamine beta-cyclodextrin is added into reaction solution
(2) (0.5g, 0.45mmol) and pyridine (10mL), N2The lower continuation room temperature of protection, which is protected from light, to be stirred to react 48 hours.Following reaction liquid
45 degree are protected from light 2 hours, and major part DMF in reaction solution is evaporated under reduced pressure and is spin-dried for complete by TLC monitoring reaction, remaining solid
It is dissolved in distilled water, stand at low temperature filtered to take filtrate after 12 hours.Filtrate is depressurized and spin-dried to slowly instilling dropwise after 15 milliliters
In 300 milliliters of acetone, precipitating is filtered to take after stirring 2 hours, precipitating is continued rear up to purer coffee with acetone washing time
Coffee acid-ethylenediamine group-beta-cyclodextrin derivative (II).(yield: 35%).1H NMR(CDCl3, 300MHz): δH, ppm 6.90
(d, 4H, J=2.4), 4.43 (m, 1H), 4.38 (m, 1H), 4.25 (t, 2H), 4.18 (m, 1H), 3.65 (t, 2H), 3.41 (m,
44H), 3.24 (s, 3H), 2.61 (m, 4H), 1.56 (m, 4H), 1.29 (m, 2H)；
The above is only section Example of the invention, not does limitation in any form to the present invention, all
It is any simple modification made according to the technical essence of the invention to above-described embodiment, equivalent variations and modification, belongs to this
Within the scope of inventive technique scheme.
Claims (2)
1. a kind antioxidant caffeic acid modification beta-cyclodextrin derivative ----caffeic acid-amido-beta-cyclodextrin derivative (I) and
Preparation method.It is characterized in that having the following general formula:
Wherein, the n indicates 0~10.
2. the derivative ----caffeic acid-amido-β-ring of kind antioxidant caffeic acid modification beta-cyclodextrin described in claim 1
The preparation method of dextrin derivative (I), it is characterised in that step and condition are as follows:
A) the compound β-CD reacts in a solvent in the presence of alkali with paratoluensulfonyl chloride, obtains mono- -6- pairs of 6- deoxidation
Tosyl group-beta-cyclodextrin (1)；Wherein, the molar ratio of β-CD and paratoluensulfonyl chloride, alkali is 1: 2~2.2: 0.1~0.2:
0.05~0.1, the reaction time is 2~6h, and reaction temperature is room temperature to 100 DEG C；
Solvent used is DMF or water or tetrahydrofuran or the common solvents such as ethyl acetate or acetone, and preferably water is as solvent；
Alkali used is organic base such as pyridine, triethylamine, DBU etc., preferably triethylamine；Or be inorganic base such as NaOH etc., preferably
NaOH；
B) compound (1) carries out amido substitution reaction in organic solvent and generates mono- 6- deoxidation-amine group-beta-cyclodextrin
It closes object (2)；Wherein, the reaction time be 6~for 24 hours, reaction temperature be room temperature to 70~100 DEG C；
Solvent used is tetrahydrofuran or alkyl halide or methanol (ethyl alcohol) or ethylenediamine, diethylenetriamine, preferably ethylenediamine etc.
Amine solvent；
C) compound (2) is reacted under the action of condensing agent with caffeic acid in organic solvent generates caffeic acid-amido-β-
Cyclodextrine derivatives (I)；Wherein, the reaction time be 2~for 24 hours, reaction temperature be room temperature to 40 DEG C；
Organic solvent used is tetrahydrofuran or alkyl halide or DMF, preferably DMF etc.；
Condensing agent used is DCC or EDCHCl/NHS etc..
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711266309.5A CN109867734A (en) | 2017-12-05 | 2017-12-05 | The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201711266309.5A CN109867734A (en) | 2017-12-05 | 2017-12-05 | The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN109867734A true CN109867734A (en) | 2019-06-11 |
Family
ID=66916306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201711266309.5A Pending CN109867734A (en) | 2017-12-05 | 2017-12-05 | The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN109867734A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108948230A (en) * | 2018-08-01 | 2018-12-07 | 陕西师范大学 | Water-soluble beta-cyclodextrin amidated derivative and synthetic method and in anti-oxidant, antibiosis application |
| CN112111025A (en) * | 2020-09-28 | 2020-12-22 | 沐荷永康生物科技(云南)有限公司 | Cannabidiol cyclodextrin conjugate and preparation method thereof |
| CN113481658A (en) * | 2021-05-27 | 2021-10-08 | 浙江工商大学 | Nano electrostatic spinning food preservative film mediated by butyl caffeate and endogenous NO type chitosan and preparation method and application thereof |
| CN113616813A (en) * | 2021-10-11 | 2021-11-09 | 奥信阳光(北京)药业科技有限公司 | Inclusion compound of ibuprofen and gallic acid modified sulfobutyl betacyclodextrin sodium |
| CN114163817A (en) * | 2021-11-10 | 2022-03-11 | 浙江大学 | Slow-release antibacterial film and preparation method thereof |
| CN114292367A (en) * | 2021-12-16 | 2022-04-08 | 厦门市建筑科学研究院有限公司 | Mud-resistant water-retaining polycarboxylate superplasticizer for machine-made sand concrete and preparation method thereof |
| CN114478937A (en) * | 2021-12-16 | 2022-05-13 | 厦门市建筑科学研究院有限公司 | Water-retaining polycarboxylate superplasticizer for machine-made sand concrete and preparation method thereof |
-
2017
- 2017-12-05 CN CN201711266309.5A patent/CN109867734A/en active Pending
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108948230A (en) * | 2018-08-01 | 2018-12-07 | 陕西师范大学 | Water-soluble beta-cyclodextrin amidated derivative and synthetic method and in anti-oxidant, antibiosis application |
| CN108948230B (en) * | 2018-08-01 | 2020-11-17 | 陕西师范大学 | Water-soluble beta-cyclodextrin amidated derivative, synthetic method and application in oxidation resistance and antibiosis |
| CN112111025A (en) * | 2020-09-28 | 2020-12-22 | 沐荷永康生物科技(云南)有限公司 | Cannabidiol cyclodextrin conjugate and preparation method thereof |
| CN112111025B (en) * | 2020-09-28 | 2022-08-16 | 云南佩林科技有限公司 | Cannabidiol cyclodextrin conjugate and preparation method thereof |
| CN113481658A (en) * | 2021-05-27 | 2021-10-08 | 浙江工商大学 | Nano electrostatic spinning food preservative film mediated by butyl caffeate and endogenous NO type chitosan and preparation method and application thereof |
| CN113616813A (en) * | 2021-10-11 | 2021-11-09 | 奥信阳光(北京)药业科技有限公司 | Inclusion compound of ibuprofen and gallic acid modified sulfobutyl betacyclodextrin sodium |
| CN114163817A (en) * | 2021-11-10 | 2022-03-11 | 浙江大学 | Slow-release antibacterial film and preparation method thereof |
| CN114163817B (en) * | 2021-11-10 | 2022-08-05 | 浙江大学 | Slow-release antibacterial film and preparation method thereof |
| CN114292367A (en) * | 2021-12-16 | 2022-04-08 | 厦门市建筑科学研究院有限公司 | Mud-resistant water-retaining polycarboxylate superplasticizer for machine-made sand concrete and preparation method thereof |
| CN114478937A (en) * | 2021-12-16 | 2022-05-13 | 厦门市建筑科学研究院有限公司 | Water-retaining polycarboxylate superplasticizer for machine-made sand concrete and preparation method thereof |
| CN114292367B (en) * | 2021-12-16 | 2024-03-01 | 厦门市建筑科学研究院有限公司 | Mud-resistant water-retaining polycarboxylate water reducer for machine-made sand concrete and preparation method thereof |
| CN114478937B (en) * | 2021-12-16 | 2024-03-01 | 厦门市建筑科学研究院有限公司 | Water-retaining polycarboxylate water reducer for machine-made sand concrete and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN109867734A (en) | The cyclodextrine derivatives and preparation method thereof of a kind of caffeic acid modification | |
| CN109867733A (en) | The cyclodextrine derivatives and preparation method thereof of a kind of ferulic acid modification | |
| Yan et al. | Preparation of N-succinyl-chitosan and their physical-chemical properties as a novel excipient | |
| CN101291957B (en) | Novel quaternary polymers | |
| WO2021013155A1 (en) | Novel glycosyl donor, preparation method therefor, and use thereof | |
| CN107021985A (en) | The synthetic method of pharmaceutical intermediate R 9 [2 (diethylphosphono methoxyl) propyl group] adenine | |
| CN106946972B (en) | A kind of ursolic acid derivative with anti-tumor activity and preparation method thereof | |
| CN106750250B (en) | Polyethylene glycol oleanolic acid derivate using amino acid as linking arm and its preparation method and application | |
| CN108863885A (en) | A kind of Ezetimibe and preparation method thereof of mono methoxy polyethylene glycol modification | |
| CN101095956B (en) | Scutellarin prodrug using carboxymethyl chitosan as the carrier and method for preparing the same | |
| CN108948230B (en) | Water-soluble beta-cyclodextrin amidated derivative, synthetic method and application in oxidation resistance and antibiosis | |
| CN103145636B (en) | 1,4-diacyl-3,6-diphenyl-1,4-dihydrotetrazine compound as well as preparation method and application thereof | |
| CN101528722B (en) | Method for preparing crystalline 3-0-alkyl-ascorbic acid | |
| CN110279869B (en) | Preparation method of glucan-quercetin prodrug polymer | |
| KR20180105450A (en) | A Method of preparing Fimarsartan choline salt and hydrate thereof | |
| CN109988297B (en) | Preparation method of alkylated pegylated oxaliplatin precursor | |
| CN110655507B (en) | Preparation method of anti-tumor medicine tegafur | |
| CN102786527B (en) | Tailed porphyrin compound modified by N1-substituted 3, 4-dihydropyrimidine-2-ketone and preparation method thereof | |
| CN105481779B (en) | Anticancer drug Rociletinib and its intermediate preparation | |
| CN104211644B (en) | A kind of synthetic method of 3,4-dichloro-pyridazine | |
| CN110903338B (en) | Sulfur-containing urea arsenic sugar with antitumor activity and preparation method and application thereof | |
| CN116655831B (en) | Preparation method of sulfobutyl-beta-cyclodextrin | |
| CN103408748B (en) | A kind of synthetic method of water-soluble pterostilbene derivative | |
| CN107382941B (en) | Flavone derivative and preparation method and application thereof | |
| JP5207165B2 (en) | Oil-soluble chitosan derivative and method for producing the same, and composition containing oil-soluble chitosan derivative |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20190611 |
|
| WD01 | Invention patent application deemed withdrawn after publication |