Home Cart Sign in  
Chemical Structure| 142168-85-2 Chemical Structure| 142168-85-2

Structure of 142168-85-2

Chemical Structure| 142168-85-2

*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 [ 142168-85-2 ]

CAS No. :142168-85-2
Formula : C8H7N3O2
M.W : 177.16
SMILES Code : O=C1N(C)C2=NC=CC=C2C(N1)=O
MDL No. :MFCD20729563

Safety of [ 142168-85-2 ]

Application In Synthesis of [ 142168-85-2 ]

* 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 [ 142168-85-2 ]

[ 142168-85-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 103976-52-9 ]
  • [ 103-71-9 ]
  • [ 142168-85-2 ]
YieldReaction ConditionsOperation in experiment
17% In toluene; at 110.0℃; for 12.0h; 2-(Methylamino)pyridine-3-carboxamide (100 mg, 0.661 mmol) and phenylisocyanate (157 mg, 1.32 mmol) were dissolved in toluene (10 mL) and stirred at 110C for 12 hours. The reaction was quenched by adding water (10 mL) and filtered to give 1-methylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (20.0 mg, as a yellow solid) with a yield of 17%. 1H NMR: (400 MHz, DMSO-d6) δ 11.72(s, 1H), 8.72(d, J = 2.0 Hz, 1H), 8.31(d, J = 7.6 Hz, 1H), 7.29(dd, J = 7.6, 2.0 Hz, 1H), 3.48(s, 3H). MS-ESI calcd. [M + H]+ 178, found 178.
17% In toluene; at 110.0℃; for 12.0h; 2-(Methylamino)pyridin-3-carboxamide (100 mg, 0.661 mmol) and phenyl isocyanate (157 mg, 1.32 mmol) were dissolved in toluene (10 mL), followed by stirring at 110 C. for 12 hours. The reaction was quenched by adding water (10 mL). The reaction solution was filtered to give 1-methylpyrido[2,3-d]pyrimidin-2,4(1H,3H)-dione (20.0 mg, yellow solid) with a yield of 17%. 1H NMR: (400 MHz, DMSO-d6) δ11.72 (s, 1H), 8.72 (d, J=2.0 Hz, 1H), 8.31 (d, J=7.6 Hz, 1H), 7.29 (dd, J=7.6, 2.0 Hz, 1H), 3.48 (s, 3H). MS-ESI calculated value: [M+H]+ 178; measured value: 178.
 

Historical Records