JP3145237B2 - Silicone hydantoin derivatives, UV absorbers and skin external preparations - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel silicone hydantoin derivative, an ultraviolet absorbent and an external preparation for skin. More specifically, the present invention relates to a novel silicone hydantoin derivative which is soluble in silicone oil, has excellent water resistance and oil resistance, and has an ultraviolet absorbing property at a wavelength in the UV-A region.

[0002]

2. Description of the Related Art Ultraviolet rays are known to cause various changes on the skin. When ultraviolet rays are classified dermatologically, long wavelength ultraviolet rays called 400-320 nm UV-A,
Medium wavelength ultraviolet light called UV-B of 320 to 290 nm,
It is divided into short wavelength ultraviolet rays called UV-C of 290 nm or less. Normally, most of the ultraviolet light to which humans are exposed is sunlight, but the ultraviolet light that reaches the ground is UV-A and UV.
At -B, UV-C is absorbed in the ozone layer and hardly reaches the ground. UV-B in ultraviolet rays reaching the ground
Causes erythema and blisters on the skin, and UV-A has been found to cause darkening of the skin and, when acted on for a long time, promotes aging of the skin.

Heretofore, a number of UV-B absorbers have been developed, but UV-A has received much attention because it has been accepted as an ultraviolet ray that makes the skin healthy brown at the seaside in summer. Did not. However, in recent years, consumer demand for white skin throughout the four seasons and the prevention of skin aging have been increased.
VA absorbers are gaining attention.

[0004] As existing UV-A absorbers, benzophenone derivatives, dibenzoylmethane derivatives, benzotriazole derivatives and the like are known, and have been used by being blended in external preparations such as cosmetics and quasi-drugs.

On the other hand, in recent years, cosmetics to which an ultraviolet absorber is blended include silicone bases such as dimethylsiloxane, which are excellent in water resistance and oil resistance, which do not easily run off due to sweat or a water bath in order to maintain their effect. It is becoming widely used. This is largely due to the water resistance and oil resistance of the silicone base, as well as the good usability such as good elongation, freshness and non-stickiness.

However, existing UV-A absorbers have extremely low compatibility with silicone bases. Therefore, an external preparation containing a silicone base is a conventional UV
It was difficult to mix the -A absorber together, and the amount used was limited to a very small amount, and there was a disadvantage that the function of the UV-A absorber was not sufficiently exhibited.

For this reason, there has been a strong demand for the development of a UV-A absorber which dissolves in a silicone base, has excellent water resistance, and protects the skin from ultraviolet rays in the UV-A region.

The present inventor has conducted intensive studies in view of such circumstances, and as a result, has found that a silicone-based hydantoin derivative is a compound that can satisfy the above properties, and has completed the present invention.

[0009]

That is, an object of the present invention is to dissolve in a silicone base,
An object of the present invention is to provide a substance that absorbs ultraviolet rays in a specific region and a skin external preparation containing the substance.

[0010]

The object of the present invention is to provide a silicone hydantoin derivative represented by the following general formula (1) , an ultraviolet absorbent comprising the silicone hydantoin derivative, and a silicone hydantoin derivative. It is achieved by a skin external preparation characterized by containing.

[0011]

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In the above general formula (1), R ¹ has 1 to ¹ carbon atoms.
An alkyl group of 4, n is 2 or 3, n + m = 3, R ² is
An alkylene group or an oxyalkylene group, X is a hydroxyl group,
C1-C8 alkyl group or C1-C8 alcohol
The xy group, a represents an integer of 0 to 5 .

Examples of R ¹ defined in the formula of the silicone-based hydantoin derivative of the present invention include methyl, ethyl,
n-propyl, isopropyl, n-butyl, isobuty
And t-butyl . R ² Examples of, for _{example, - (CH 2) -,} - (CH 2) 2 -, - (CH 2)
_{3 -, - CH 2 CH (} CH 3) CH 2 -, - CH 2 CH
_{2 CH (CH 3) -,} - CH (CH 3) CH 2 CH 2
_{-, - C (CH 3)} 2 CH 2 CH 2 -, - (CH 2) 5
_{-, - CH 2 CH 2 CH} 2 CH (CH 2 CH 3) -, -
_{CH 2 CH 2 CH 2 CH 2} CH (CH 3) -, - (CH
_{2) 7 -, - CH 2} CH 2 OCH 2 CH 2 -, - CH 2 C
H ₂ CH ₂ OCH ₂ -, and the like. Examples of X include methoxy, ethoxy, isopropoxy, butoxy,
t-butoxy, hexyloxy, octyloxy and the like. a represents the number of substitutions of X and is an integer of 0 to 5.

The silicone-based hydantoin derivative of the present invention can be produced, for example, by the following method.

[0015]

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The benzaldehyde derivative (2) and the hydantoin (3) are prepared in the presence of an amino acid such as glycine or alanine or a salt thereof in water or an aqueous solution at room temperature to 150 ° C.
In 20 hours was reacted after obtaining (4), (4) a N, N- dimethylformamide, in a solvent such as dimethyl sulfoxide, KOH, NaOH, the presence of a base such as K ₂ CO ^3, silicone Compound A ( a compound represented by the following chemical formula 4)
Wherein R ¹ is an alkyl group having 1 to 4 carbon atoms, and R ² is
A alkylene group or an oxyalkylene group, and B is a halogen atom
And Br, Cl, I, etc. Also, n is 2 or
3, n + m = 3 . ) And room temperature to 200 ° C for 5 minutes to 5
By reacting for 0 hour, (1) can be obtained.

[0017]

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The base used for the external preparation for skin of the present invention may be any base as long as the silicone-based hydantoin derivative can be dissolved.
Refreshing feeling, non-greasy feeling and excellent water resistance,
Oil resistance is preferred, and furthermore, functions such as hardly flowing into sweat and water are obtained, which is preferable.

The silicone base is not particularly limited,
For example, chain polysiloxanes such as dimethylpolysiloxane, methylpolysiloxane and methylhydrogenpolysiloxane, cyclic polysiloxanes such as decamethylpolysiloxane, dodecamethylpolysiloxane, tetramethyltetrahydrogenpolysiloxane, and polyether fatty acid-modified polysiloxane And higher alcohol-modified polysiloxanes and amino acid-modified polysiloxanes.

The external preparation for skin of the present invention includes other components usually used in external preparations for skin such as cosmetics and quasi-drugs,
For example, oil, lubricating oil, ultraviolet absorbers other than the present invention, antioxidants, surfactants, preservatives, sequestering agents, fragrances,
Water, alcohol, a thickener, and the like can be appropriately added as needed. The external preparation for skin of the present invention is not particularly limited in its application field, and can be used in cosmetics, quasi-drugs, and the like according to the characteristics and purpose of the silicone-based hydantoin derivative used in the present invention.

Here, the dosage form of the external preparation for skin of the present invention is arbitrary, and any dosage form such as powder, cream, paste, stick, liquid, spray, foundation and the like may be used. It may be emulsified into a W / O type or an O / W type using an emulsifier. The compounding amount varies depending on the above-mentioned dosage form, but is generally 0.1 to 30% by weight.
And more preferably 0.2 to 20% by weight.

[0022]

The present invention will be further described with reference to the following examples. The present invention is not limited by these.

Example 1 (1) 3,3.0-dimethoxybenzaldehyde 83.0
g, 50.0 g of hydantoin, 28.1 g of glycine, 7.5 g of sodium hydroxide and 200 ml of water were stirred at about 75 ° C. for 8 hours. After cooling, the obtained crystals were collected by filtration, washed with water, and dried to obtain 112.4 g of 5- (3,4-dimethoxybenzylidene) hydantoin (Formula 5 ) (yield: 90.6%).

[0024]

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(2) N, N-dimethylformamide (D
In 50 ml of MF) 12.40 g of the above 5- (3,4-dimethoxybedylidene) hydantoin, 16.42 g of a silicone compound represented by the following formula 6 , and anhydrous potassium carbonate 4.1.
5 g was added, and the mixture was stirred at about 100 ° C. for 3 hours.

[0026]

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(3) After cooling, insolubles were filtered off and DMF was distilled off under reduced pressure to obtain a pale yellow solid. The solid was recrystallized from methanol, a silicone-based hydantoin derivatives 17.93G (yield 70 of the present invention represented by the following formula 7.
3%).

[0028]

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[0029] Example 2 (1) except for changing the silicone compound of 6 to silicone compounds 20.48g represented by the following formula 8 was reacted analogously as described in Example 1,

[0030]

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(2) 18.02 g (yield: 61.7) of the silicone-based hydantoin derivative of the present invention represented by the following formula ( 9 ):
%).

[0032]

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[0033] Example 3 (1) except for changing the silicone compound of 6 to silicone compounds 17.19g represented by the following formula 10 was reacted analogously as described in Example 1,

[0034]

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[0035] (2) Silicone-based hydantoin derivatives of the present invention represented by the following formula 11 19.13G (yield 73.
0%).

[0036]

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[0037] Example 4 (1) except for changing the silicone compound of 6 to silicone compounds 17.19g represented by Formula 12 was reacted analogously as described in Example 1,

[0038]

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[0039] (2) Silicone-based hydantoin derivatives of the present invention represented by Formula 13 17.95 g (yield: 68.
5%).

[0040]

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[0041] Example 5 (1) except for changing the silicone compound of 6 to silicone compounds 17.96g represented by Formula 14 was reacted analogously as described in Example 1,

[0042]

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[0043] (2) Silicone-based hydantoin derivatives of the present invention represented by Formula 15 17.40 g (yield 64.
7%).

[0044]

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Example 6 (1) 3,4-dimethoxybenzaldehyde was converted to 3,4
The reaction was carried out in the same manner as in Example 1 except that the amount was changed to 98.0 g of 5-trimethoxybenzaldehyde, and 5- (3,4,5-
Trimethoxy benzylidene) hydantoin (of 16) 1
28.0 g (92.1% yield) were obtained.

[0046]

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(2) The reaction was carried out according to Example 1, except that 5- (3,4,5-trimethoxybenzylidene) hydantoin was changed to 13.90 g of 5- (3,4,5-trimethoxybenzylidene) hydantoin. silicone hydantoin derivatives of the present invention represented by Formula 17 20.60Gg
(Yield: 76.3%).

[0048]

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It should be noted that Chemical Formula 7 , Chemical Formula 9 , Chemical Formula 11 , Chemical Formula 13 , Chemical Formula 1
5. The structure of Chemical formula 17 was confirmed by a ¹ H-NMR spectrum, an infrared absorption spectrum and an MS spectrum.

The ¹ H-NMR spectrum was measured by JNM FX-
The measurement was performed using 270 (manufactured by JEOL Ltd.) with CDCl ₃ as the solvent (internal standard CHCl 3). As a representative example, FIG. 1 shows a ¹ H-NMR spectrum of Chemical Formula 7 .

The infrared absorption spectrum was measured by a potassium bromide tablet method using a 270-30 infrared spectrophotometer (manufactured by Hitachi, Ltd.). As a typical example, FIG. 2 shows an infrared absorption spectrum of Chemical formula 7 .

The MS spectrum was obtained from JMSDX-303.
(Manufactured by JEOL Ltd.) using the EI method. In each case, a molecular ion peak (M ⁺ ) was confirmed.

For the compounds obtained in Examples 1 to 6, UV
When an ultraviolet absorption spectrum was measured with an ethanol solvent using a -200 type spectrophotometer (manufactured by Shimadzu Corporation),
All showed maximum absorption in the UV-A region. From this, it can be said that the silicone-based hydantoin derivative of the present invention is an excellent UV-A absorber. As a representative example, FIG.
2 shows an ultraviolet absorption spectrum of Chemical Formula 7 .

The solubility of the silicone-based hydantoin derivative of the present invention in a silicone-based material was tested at 25 ° C. in dimethylpolysiloxane and methylphenylpolysiloxane. In each case, 10% by weight or more was dissolved, showing excellent solubility.

The water resistance and oil resistance were as follows. The silicone hydantoin derivative of the present invention was mixed with oil such as water, 50% ethanol, liquid paraffin, and the like, and allowed to stand at 50 ° C. for 60 days. As a result, it was confirmed that hydrolysis and the like did not occur and that water resistance and oil resistance were excellent.

Example 7 Sunscreen cosmetics (oil type) (1) 48.0 parts by weight of decamethylcyclopentasiloxane (2) Dimethylpolysiloxane (10 cs / 25 ° C.) 20.0 (3) Methylphenylpolysiloxane ( (20 cs / 25 ° C.) 20.0 (4) Silicone resin 10.0 (5) Silicone hydantoin derivative (compound of Example 1) 2.0

(Preparation method) (1) to (5) were mixed and dissolved sufficiently, followed by filtration to obtain a product.

Comparative Example 1 A product was obtained in the same manner as in Example 7 except that (5) was omitted from the formulation of Example 7.

Example 8 Sunscreen cosmetics (cream) (1) 9.0 parts by weight of decamethylpentasiloxane (2) Liquid paraffin 3.0 (3) Isopropyl myristate 2.0 (4) Vaseline 5.0 ( 5) Cetanol 5.0 (6) Stearic acid 3.0 (7) Glyceryl monoisostearate 3.0 (8) Silicone hydantoin derivative (compound of Example 2) 2.0 (9) Preservative 0.2 (10) Fragrance 0.2 (11) Glycerin 10.0 (12) Propylene glycol 5.0 (13) Potassium hydroxide 0.2 (14) Purified water 52.4

(Production method) (1) to (10) were heated and stirred at 70 ° C. to obtain an oil phase. After heating (11) to (14) to 70 ° C. and completely dissolving them, they were made into an aqueous phase. The oil phase was added to the aqueous phase and emulsified by an emulsifier. The emulsion was cooled to 30 ° C. to obtain a product.

Comparative Example 2 A product was obtained in the same manner as in Example 8 except that (8) was omitted from the formulation of Example 8.

Example 9 Sunscreen lotion (1) 10.0 parts by weight of dimethylpolysiloxane (5 cs / 25 ° C.) (2) methylphenylpolysiloxane (20 cs / 25 ° C.) 7.0 (3) Stearic acid 1.0 (4) Silicone hydantoin derivative (compound of Example 3) 10.0 (5) Preservative 0.2 (6) Fragrance 0.2 (7) Glycerin 5.0 (8) Potassium hydroxide 0.2 (9) ) Purified water 66.4

(Production method) (1) to (6) were heated and stirred at 70 ° C. to obtain an oil phase. After heating (7) to (9) to 70 ° C. and completely dissolving the mixture, the mixture was treated as an aqueous phase. The oil phase was added to the aqueous phase and emulsified by an emulsifier. The emulsion was cooled to 30 ° C. to obtain a product.

Comparative Example 3 A product was obtained in the same manner as in Example 9 except that (4) was omitted from the formulation of Example 9.

With respect to Examples 7 to 9 and Comparative Examples 1 to 3 obtained as described above, the effect of preventing ultraviolet rays was measured. The measuring method was as follows. The above-mentioned cosmetic containing the product of the present invention was applied to the back of a person in an amount of ² mg / cm ² , and 15 minutes later, UV-A irradiation was performed. UV-A irradiation is performed using a BLB lamp at 365 nm,
Ultraviolet rays having an energy amount of 9 J / cm ² were irradiated, and the minimum blackening amount (MMD) was determined using the following equation.

[0066]

(Equation 1)

Table 1 shows the results.

[0068]

[Table 1]

As can be seen from Table 1, the MMD values of the examples are higher than those of the comparative examples. That is, it is understood that an excellent ultraviolet ray preventing effect can be obtained by blending the silicone hydantoin derivative of the present invention.

[0070]

The silicone hydantoin derivative of the present invention is an excellent ultraviolet absorber having a maximum absorption in the UV-A region. Further, the ultraviolet absorber of the present invention has water resistance,
Because it has excellent oil resistance, it can provide an external preparation for the skin in which the base and other components can be freely selected, and at the same time, is excellent even when exposed to severe conditions under the scorching sun as a sunscreen cosmetic. It is clear that it shows an effect.

[Brief description of the drawings]

FIG. 1 is a diagram showing a ¹ H-NMR spectrum of a silicone-based hydantoin derivative 7 obtained in Example 1 of the present invention.

FIG. 2 is a view showing an infrared absorption spectrum of a silicone-based hydantoin derivative 7 obtained in Example 1 of the present invention.

FIG. 3 is a view showing an ultraviolet absorption spectrum of a silicone-based hydantoin derivative 7 obtained in Example 1 of the present invention.

Claims (3)

(57) [Claims] 1. A compound of the general formula (1) ( Wherein, R ¹ is an alkyl group having 1 to 4 carbon atoms, and n is
2 or 3, n + m = 3, R 2 is an alkylene group or an oxyalkylene group, X is a hydroxyl group, an alkyl group or an alkoxy group having 1 to 8 carbon atoms having 1 to 8 carbon atoms, a is an integer of 0 to 5 . A silicone-based hydantoin derivative represented by the formula: 2. An ultraviolet absorbent comprising the silicone-based hydantoin derivative according to claim 1. 3. An external preparation for skin comprising the silicone-based hydantoin derivative according to claim 1.