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Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate

Product Name
Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate
CAS No.
402948-37-2
Chemical Name
Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate
Synonyms
CHIR161527;Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate;Ethyl 2-[6-(4-Methyl-1-piperazinyl)-2-benzimidazolyl]acetate;ETHYL 2-[5-(4-METHYLPIPERAZINYL)BENZO[D]IMIDAZOL-2-YL]ACETATE;Ethyl [6-(4-methyl-1-piperazinyl)-1H-benzimidazol-2-yl]acetate;ethyl 2-(5-(4-Methylpiperazin-1-yl)-1H-benzo[d]iMidazol-2-yl)acetate;ethyl 2-(6-(4-Methylpiperazin-1-yl)-1H-benzo[d]iMidazol-2-yl)acetate;1H-Benzimidazole-2-acetic acid, 6-(4-methyl-1-piperazinyl)-, ethyl ester;6-(4-methyl-piperazin-1-yl)-1H-benzoimidazol-2-yl]-acetic acid ethyl ester
CBNumber
CB01512663
Molecular Formula
C16H22N4O2
Formula Weight
302.37
MOL File
402948-37-2.mol
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Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate Property

Boiling point:
516.4±50.0 °C(Predicted)
Density 
1.220±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
12.47±0.10(Predicted)
Appearance
White to yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H411Toxic to aquatic life with long lasting effects

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N-Bromosuccinimide Price

AK Scientific
Product number
4808BB
Product name
Ethyl2-(5-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)acetate
Packaging
100mg
Price
$128
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0377371
Product name
ETHYL-2-(6-(4-METHYLPIPERAZIN-1-YL)-1H-BENZO[D]IMIDAZOL-2-YL)ACETATE
Purity
95.00%
Packaging
5MG
Price
$505.89
Updated
2021/12/16
Ambeed
Product number
A108739
Product name
Ethyl2-(5-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)acetate
Purity
97%
Packaging
100mg
Price
$51
Updated
2021/12/16
Ambeed
Product number
A108739
Product name
Ethyl2-(5-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)acetate
Purity
97%
Packaging
250mg
Price
$105
Updated
2021/12/16
Crysdot
Product number
CD11128682
Product name
Ethyl2-(5-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)acetate
Purity
97%
Packaging
1g
Price
$258
Updated
2021/12/16
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Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate Chemical Properties,Usage,Production

Synthesis

27317-59-5

23491-48-7

402948-37-2

General procedure for the synthesis of ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate from ethyl 3-ethoxy-3-iminopropionate and 5-(4-methylpiperazinyl)-2-nitroaniline: 43 mmol of 5-(4-methylpiperazin-1-yl)-2-nitroaniline (compound b) was dissolved in 150 mL of anhydrous ethanol, and then loaded after sufficient dissolution into the first raw material storage tank 1; in the second raw material storage tank 2, 20 mL of 3.6% by weight HCl was dissolved in 150 mL of anhydrous ethanol; 65 mmol of β-ethoxy-β-imino-propionic acid ethyl ester hydrochloride (Compound c) was dissolved in 150 mL of ethanol, and was loaded into the third raw material storage tank 3 after being fully dissolved. At this time, the molar ratio of 5-(4-methylpiperazin-1-yl)-2-nitroaniline to β-ethoxy-β-imino-propionic acid ethyl ester hydrochloride was 1:1.5. The solutions in the first raw material storage tank 1 and the second raw material storage tank 2 were simultaneously pumped into the reaction device, and passed through the first microstructured mixer 4 into the first microstructured reactor (Reactor 1) having an inner diameter of 0.5 mm and a volume of 50 mL Perform the reaction. The microreactor parameters were set: a continuous flow rate of 1.4 mL/min in the first step, a reaction temperature of 80°C, and a residence time of 8 min, and the reaction mainly produced the intermediate 4-(4-methylpiperazin-1-yl)isophthalamide. Subsequently, the solution in the third raw material storage tank 3 and the reaction solution obtained in the reactor 1 were simultaneously pumped into the second microstructure mixer 5, and entered into the second microstructure reactor (reactor 2) with an inner diameter of 0.5 mm and a volume of 50 ml to carry out the mixing reaction. The microreactor parameters were set: continuous flow rate of 3 mL/min for the second step, reaction temperature of 80°C, and residence time of 20 min. After completion of the reaction, the reaction solution was concentrated to obtain an oily substance, which was solubilized with 15 mL of water, extracted several times with CH2Cl2, the organic phases were combined, and the solvent was evaporated to obtain the orange-colored oily substance, i.e., compound d, with a yield of 91%.

References

[1] Patent: CN108610293, 2018, A. Location in patent: Paragraph 0032; 0039-0044; 0048; 0050; 0052; 0054; 0056

Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate manufacturers

Nanjing Fred Technology Co., Ltd
Product
Ethyl2-(5-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)acetate 402948-37-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1 ton
Release date
2023-12-28

402948-37-2, Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetateRelated Search:


  • ethyl 2-(6-(4-Methylpiperazin-1-yl)-1H-benzo[d]iMidazol-2-yl)acetate
  • ethyl 2-(5-(4-Methylpiperazin-1-yl)-1H-benzo[d]iMidazol-2-yl)acetate
  • CHIR161527
  • ETHYL 2-[5-(4-METHYLPIPERAZINYL)BENZO[D]IMIDAZOL-2-YL]ACETATE
  • Ethyl 2-[5-(4-methylpiperazinyl)benzimidazol-2-yl]acetate
  • Ethyl [6-(4-methyl-1-piperazinyl)-1H-benzimidazol-2-yl]acetate
  • 6-(4-methyl-piperazin-1-yl)-1H-benzoimidazol-2-yl]-acetic acid ethyl ester
  • 1H-Benzimidazole-2-acetic acid, 6-(4-methyl-1-piperazinyl)-, ethyl ester
  • Ethyl 2-[6-(4-Methyl-1-piperazinyl)-2-benzimidazolyl]acetate
  • 402948-37-2
  • API intermediates