Home Cart Sign in  
Chemical Structure| 218594-00-4 Chemical Structure| 218594-00-4

Structure of 218594-00-4

Chemical Structure| 218594-00-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 218594-00-4 ]

CAS No. :218594-00-4
Formula : C23H18N2O
M.W : 338.40
SMILES Code : O=CC1=CN(N=C1)C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
MDL No. :MFCD23135632

Safety of [ 218594-00-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 218594-00-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 218594-00-4 ]

[ 218594-00-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 68-12-2 ]
  • [ 191980-54-8 ]
  • [ 218594-00-4 ]
  • 2
  • [ 76-83-5 ]
  • [ 35344-95-7 ]
  • [ 218594-00-4 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 20℃; for 1h; [007101 Compound 80 was prepared in 4 steps from 1 H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> according to the following procedures: <strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> (2.1 mmol, 1.0 equiv) was dissolved in 20 mL methylene chloride followed by the addition of triethylamine (3.0 equiv) and trityl chloride (1.0 equiv). The reaction was stirred at RT for lh after it was quenched with water (lmL) and extrated with methylene chloride. The organic layers were concentrated and purified using flash silica gel chromatography (gradient 0-30percent methanol/methylene chloride with 0.5percent triethylamine). 1-Trity -]H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> was then converted to it?s corresponding alkyne using Method J after which it was coupled to compound B using the analogous coupling conditions in Example 1. The resulting compound was then deprotected under standard triflouroacetic acid in methylene chloride deprotection conditions after which it was concentrated and purified using flash silica gel chromatography (ISCO, gradient 0-5percent methanol/methylene chroride with 0.05percent triethylamine and then repurified using reverse-phase HPLC (Interchim Cl 8-Sunfire column, gradient of acetonitrile/water with 0.01percent formic acid) to provide compound 80. ESI-MS m/z: 515.0 [M+H]b.
With triethylamine; In dichloromethane; at 20℃; for 1h; [001366] Compound 80 was prepared in 4 steps from lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> according to the following procedures: lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> (2.1 mmol, 1.0 equiv) was dissolved in 20 mL methylene chloride followed by the addition of triethylamine (3.0 equiv) and trityl chloride (1.0 equiv). The reaction was stirred at RT for lh after it was quenched with water (ImL) and extrated with methylene chloride. The organic layers were concentrated and purified using flash silica gel chromatography (gradient 0-30percent methanol/methylene chloride with 0.5percent triethylamine). 1-Trity -/H-pyrazole-4- carbaldehyde was then converted to it's corresponding alkyne using Method J after which it was coupled to compound B using the analogous coupling conditions in Example 1. The resulting compound was then deprotected under standard triflouroacetic acid in methylene chloride deprotection conditions after which it was concentrated and purified using flash silica gel chromatography (ISCO, gradient 0-5percent methanol/methylene chroride with 0.05percent triethylamine and then repurified using reverse-phase HPLC (Interchim C18-Sunfire column, gradient of acetonitrile/water with 0.01percent formic acid) to provide compound 80. ESI-MS m/z: 515.0 [M+H]+.
 

Historical Records

Technical Information

Categories