4, 5-disubstituted-2-aminothiazole compound and preparation method thereof

An aminothiazole and compound technology, applied in the field of compound synthesis, can solve the problems of poor applicability of different functional groups, difficult to obtain raw materials, difficult to obtain raw materials, etc., and achieves the effects of less environmental pollution, high yield, and easy availability of raw materials

Inactive Publication Date: 2014-11-19
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] Although there are many reports on the synthesis of 2-aminothiazole, the known synthesis methods still have problems such as difficult acquisition of raw materials, low product yield, poor applicability to different functional groups, and cumbersome operations.
In addition, the above method usually introduces an alkyl group, aryl group, hydrogen or alkoxy group at the 4-position of the thiazole ring, and there are few reports on the introduction of an acyl group or alkoxycarbonyl group at the 4-position of the thiazole ring.
[0010] The known method of introducing an acyl or alkoxycarbonyl group at the 4-position of the thiazole ring is...

Method used

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  • 4, 5-disubstituted-2-aminothiazole compound and preparation method thereof
  • 4, 5-disubstituted-2-aminothiazole compound and preparation method thereof
  • 4, 5-disubstituted-2-aminothiazole compound and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Embodiment 1, 4-(4-chlorobenzoyl)-5-phenyl-2-aminothiazole (m1)

[0050] Add 141.9 mg (0.5 mmol) of 1-p-chlorophenyl-2-azido-3-phenyl-2-propen-1-one and 97.2 mg (1 mmol) of potassium thiocyanate to the reaction flask, and then add CH 3 CH 2 CH 2 OH (n-propanol) 2.0ml, ferrous sulfate heptahydrate 69.5mg (0.25mmol), after the addition is complete, stir and react at 80°C for 12 hours, TLC detects the reaction (petroleum ether: ethyl acetate = 1:1 volume ratio) .

[0051] Remarks: When TLC detection shows that 1-p-chlorophenyl-2-azido-3-phenyl-2-propen-1-one disappears, it means that the reaction has ended.

[0052] After the reaction was completed, concentrate to remove n-propanol, cool to room temperature, add 60ml of water, and extract the reaction solution three times with 3×20mL ethyl acetate, and wash the organic layer (at the upper layer) with 3×30mL saturated brine three times after merging, and then use Anhydrous sodium sulfate (2.0g) was dried for 30 minutes...

Embodiment 2

[0077] Embodiment 2, 4-benzoyl-5-phenyl-2-aminothiazole (m2)

[0078] Replace 1-p-chlorophenyl-2-azido-3-phenyl-2-propen-1-one with 1-phenyl-2-azido-3-phenyl-2-propen-1-one, mol Quantity is constant, all the other are equal to embodiment 1. 128.8 mg of the product 4-benzoyl-5-phenyl-2-aminothiazole was obtained as a yellow solid, with a yield of 92%.

[0079] Its structural formula is:

[0080]

[0081] Yellow solid; mp:160.4-160.8℃; 1 H NMR (500MHz, DMSO) δ7.84(d, J=7.05, 2H), 7.59(t, J=6.88, 1H), 7.47(d, J=7.31, 2H), 7.35-7.24(m, 7H) ; 13 C NMR (125MHz, DMSO) δ190.76, 166.14, 143.60, 137.12, 133.12, 131.11, 129.66, 128.99, 128.56, 128.39, 128.35, 127.59; HRMS (ESI): m / zcalcd for C 16 h 12 N 2 OS[M+H] + :281.0749,found:281.0748.

Embodiment 3

[0082] Example 3, 4-(4-methylbenzoyl)-5-phenyl-2-aminothiazole (m3)

[0083] Replace 1-p-chlorophenyl-2-azido-3-phenyl-2-propene-1-one with 1-p-methylphenyl-2-azido-3-phenyl-2-propene-1-one Ketone, molar weight is constant, all the other are equal to embodiment 1. 138.2 mg of the product 4-(4-methylbenzoyl)-5-phenyl-2-aminothiazole was obtained as a yellow solid, with a yield of 94%.

[0084] Its structural formula is:

[0085]

[0086] Yellow solid; mp:189.4-189.9℃; 1 H NMR (500MHz, DMSO) δ7.75 (d, J=8.07, 2H), 7.33 (s, 2H), 7.28-7.21 (m, 7H), 2.35 (s, 3H); 13C NMR (125MHz, DMSO) δ190.63, 166.21, 143.88, 143.74, 134.45, 131.18, 129.85, 128.98, 128.60, 128.19, 127.91, 127.47, 21.22; HRMS (ESI): m / z calcd for C 17 h 14 N 2 OS[M+H] + :295.0905,found:295.0907.

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Abstract

The invention discloses a 4, 5-disubstituted-2-aminothiazole compound. The structural formula is shown in the specification, wherein R1 is 4-tolyl, 4-chlorophenyl, 4-methoxyphenyl, 4-nitrobenzene or propoxy, and R2 is phenyl, 4-tolyl, 4-fluorophenyl, 4-methoxyphenyl, 2-furyl, isopropyl, 4-nitrophenyl or n-propyl. The invention simultaneously provides a preparation method of the 4, 5-disubstituted-2-aminothiazole compound. The preparation method comprises the following steps: enabling an olefin azide type compound and potassium thiocyanate to react at the temperature of 75-85 DEG C in the presence of a solvent and a metal catalyst, concentrating an obtained reaction solution, then extracting with water and ethyl acetate, washing an obtained organic layer, then drying and concentrating by a rotary evaporator; performing silica gel column chromatography on an obtained concentrate to obtain the 4, 5-disubstituted-2-aminothiazole compound.

Description

technical field [0001] The invention belongs to a synthesis method of a compound, and mainly relates to a 4,5-disubstituted-2-aminothiazole compound and a preparation method thereof. Background technique [0002] Thiazole compounds are an important class of heterocyclic compounds, which have important applications in the fields of medicine, agriculture, materials, and life sciences. Aminothiazole compounds can undergo a series of reactions through the amino functional group, and the compounds thus synthesized have a wide range of applications in pesticides, dyes, etc., such as for the synthesis of herbicides, monoazo disperse dyes, etc. 2-aminothiazole compounds are widely used in the synthesis of drugs for the treatment of tumors, hypertension and other diseases. [0003] 2-Aminothiazole compounds have received extensive attention because of their important application value, and the most classic one is the thiazole synthesis method proposed by Hantzsch (Hantzsch, A.; Webe...

Claims

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Application Information

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IPC IPC(8): C07D277/40C07D417/04C07D277/56A61P35/00
CPCC07D277/40C07D277/56C07D417/04
Inventor 章国林陈斌辉倪航程俞永平
Owner ZHEJIANG UNIV
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