Home Cart Sign in  
Chemical Structure| 180869-39-0 Chemical Structure| 180869-39-0

Structure of 180869-39-0

Chemical Structure| 180869-39-0

*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 [ 180869-39-0 ]

CAS No. :180869-39-0
Formula : C6H7N3O
M.W : 137.14
SMILES Code : O=CC1=NC(NC)=NC=C1
MDL No. :MFCD09999147
InChI Key :HGTHYMOKILRDHL-UHFFFAOYSA-N
Pubchem ID :22002531

Safety of [ 180869-39-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 180869-39-0 ]

* 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 [ 180869-39-0 ]

[ 180869-39-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 180869-38-9 ]
  • [ 180869-39-0 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In water; at 48℃; for 17h; Step [B] : Preparation of 2-methylamino-pyrimidine-4- carbaldehyde (4-Dimethoxymethyl-pyrimidin-2-yl) -methylamine (Step A, 3.60 g, 19.6 mmol) and 3 N HCl (14.4 mL, 43.2 mmol) were combined and stirred at [48 C] for 17 h. After cooling to RT, 4.3 g of [NAHC03] was added in portions. The mixture was extracted with EtOAc, the combined organic portions were dried over [MGSO4,] filtered, and condensed to give the titled compound as a yellow solid. MS [(ES+)] : 138.3 (M+H) +. Calc'd for [C6H7N30-137.] 14.
With hydrogenchloride; at 60℃; for 2h; To the 2M solution of methylamine in THF (3 mL) 232 mg 4-(dimethoxymethyl)-2- methylsulfonyl-pyriinidine (Preparation 9a3, 1.00 mmol) was added and it was stirred at room temperature for lh. The reaction mixture was concentrated under reduced pressure, the residue was diluted with EtOAc and washed with brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure. To the residue 3 mE 2N HC1 was added and it was stilTed at 60C for 2h. Than it was cooled to 0C, the pH was adjusted to 9 using 2N NaOH solution, and then 76 mg sodium borohydride (2.0 mmol) was added and the mixture was stirred for lh. The reaction mixture was extracted with EtOAc, thecombined organic layers were dried over MgSO4 and concentrated under reduced pressure to give the title product.MS: (M+2H) 141.4.
 

Historical Records

Technical Information

Categories