ChemicalBook > CAS DataBase List > 2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE

2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE

Product Name
2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE
CAS No.
195053-92-0
Chemical Name
2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE
Synonyms
4-(2-Aminoethyl)-1-tritylimidazole;2-(1-tritylimidazol-4-yl)ethanamine;2-(1-Trityl-1H-iMidazol-4-yl)ethanaMine;2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE;N'-(3,4-dichlorophenyl)propane-1,5-diamine;2-(1-trityl-1H-imidazol-4-yl)ethan-1-amine;1-(Triphenylmethyl)-1H-Imidazole-4-ethanamine;1H-Imidazole-4-ethanamine, 1-(triphenylmethyl)-;2-(1-Trityl-1H-iMidazol-4-yl)ethanaMine hydrate;2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE
CBNumber
CB7119428
Molecular Formula
C24H23N3
Formula Weight
353.46
MOL File
195053-92-0.mol
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2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE Property

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
Off-white to light yellow Solid
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Safety

RIDADR 
3259
HazardClass 
8
PackingGroup 
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0018561
Product name
2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE
Purity
95.00%
Packaging
1G
Price
$909.56
Updated
2021/12/16
AK Scientific
Product number
1017AJ
Product name
2-(1-Trityl-1H-imidazol-4-yl)-ethylaminehydrate
Packaging
5g
Price
$1072
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0018561
Product name
2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE
Purity
95.00%
Packaging
5G
Price
$1485.62
Updated
2021/12/16
Chemenu
Product number
CM117874
Product name
4-(2-Aminoethyl)-1-tritylimidazole
Purity
95+%
Packaging
250mg
Price
$52
Updated
2021/12/16
Crysdot
Product number
CD11174404
Product name
2-(1-Trityl-1H-imidazol-4-yl)ethanamine
Purity
97%
Packaging
250mg
Price
$64
Updated
2021/12/16
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2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE Chemical Properties,Usage,Production

Synthesis

312937-01-2

195053-92-0

Histamine dihydrochloride (20.47 g, 0.111 mol) was used as starting material and stirred with triethylamine (48 mL, 0.345 mol) in anhydrous methanol (400 mL) for 10 min at room temperature. Subsequently, a solution of ethyl trifluoroacetate (14.6 mL, 0.122 mol) in methanol (30 mL) was added slowly and dropwise over a period of 30 min at 0 °C. The reaction mixture was continued to be stirred at room temperature for 3.5 hours before the solvent was removed by vacuum evaporation. The residue was dissolved in dichloromethane (450 mL) and triethylamine (31 mL, 0.222 mol) was added. Next, triphenylmethyl chloride (34.1 g, 0.122 mol) was added in batches and the mixture was stirred overnight at room temperature. Upon completion of the reaction, chloroform (400 mL) and water (600 mL) were added to the mixture, the aqueous layer was separated and extracted with chloroform (3 x 400 mL). The organic layers were combined and dried with anhydrous magnesium sulfate. After evaporation of the solvent, the resulting beige solid was ground with hexane (1000 mL) and filtered to afford 2,2,2-trifluoro-N-[2-(1-trityl-1H-imidazol-4-yl)-ethyl]-acetamide as a white solid in a yield of 45.54 g (91% yield).1H NMR (300 MHz, CDCl3, δH): 8.44 (bs, 1H) , 7.43 (s, 1H), 7.41-7.33 (m, 9H), 7.19-7.10 (m, 6H), 6.65 (s, 1H), 3.66 (q, J = 5.9 Hz, 2H), 2.79 (t, J = 5.9 Hz, 2H). The above amide (45.54 g, 0.101 mol) was dissolved in tetrahydrofuran (1000 mL) and methanol (1200 mL) and a solution of sodium hydroxide (20.26 g, 0.507 mol) in water (500 mL) was added. The mixture was stirred at room temperature for 2 hours and then concentrated. The residue was partitioned between chloroform (1200 mL) and water (800 mL) and the aqueous layer was extracted with chloroform (3 x 400 mL). The organic layers were combined, dried with anhydrous magnesium sulfate and the solvent was evaporated to give a brown oil, which was dried for 3 days to give the title product 2-(1-trityl-1H-imidazol-4-yl)ethylamine as a beige solid in a yield of 32.23 g (90% yield), 82% total yield. Melting point: 111-113 °C. 1H NMR (300 MHz, CDCl3, δH): 7.39 (d, J = 1.3 Hz, 1H), 7.38-7.32 (m, 9H), 7.20-7.12 (m, 6H), 6.61 (s, 1H), 3.00 (t, J = 6.6 Hz, 2H), 2.70 (t, J = 6.5 Hz , 2H), 1.93 (bs, 2H).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 9, p. 1269 - 1273
[2] Patent: EP3000482, 2016, A1. Location in patent: Paragraph 0261; 0263
[3] Patent: US2010/216854, 2010, A1. Location in patent: Page/Page column 24
[4] Patent: US6562823, 2003, B1
[5] Journal of Biological Inorganic Chemistry, 2016, vol. 21, # 5-6, p. 777 - 792

2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE Preparation Products And Raw materials

Raw materials

Preparation Products

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195053-92-0, 2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATERelated Search:


  • 2-(1-Trityl-1H-iMidazol-4-yl)ethanaMine hydrate
  • 2-(1-Trityl-1H-iMidazol-4-yl)ethanaMine
  • 1H-Imidazole-4-ethanamine, 1-(triphenylmethyl)-
  • 1-(Triphenylmethyl)-1H-Imidazole-4-ethanamine
  • 2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE
  • 2-(1-TRITYL-1H-IMIDAZOL-4-YL)-ETHYLAMINE HYDRATE
  • 2-(1-tritylimidazol-4-yl)ethanamine
  • 2-(1-trityl-1H-imidazol-4-yl)ethan-1-amine
  • N'-(3,4-dichlorophenyl)propane-1,5-diamine
  • 4-(2-Aminoethyl)-1-tritylimidazole
  • 2-(1-Trityl-1H-imidazol-4-yl)-ethylamine, CAS 195053-92-0
  • 195053-92-0
  • C24H23N3
  • C24H23N3H2O