Home Cart Sign in  
Chemical Structure| 62484-22-4 Chemical Structure| 62484-22-4

Structure of 62484-22-4

Chemical Structure| 62484-22-4

*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 [ 62484-22-4 ]

CAS No. :62484-22-4
Formula : C8H5ClN2O2
M.W : 196.59
SMILES Code : O=C(N1)NC2=C(C=CC=C2Cl)C1=O
MDL No. :MFCD09954846

Safety of [ 62484-22-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 62484-22-4 ]

* 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 [ 62484-22-4 ]

[ 62484-22-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 62484-22-4 ]
  • [ 62484-29-1 ]
YieldReaction ConditionsOperation in experiment
76% With trichlorophosphate; for 16h;Reflux; (1041) To the compound 77 (3.8 g, 19.33 mmol), 60 mL POCl3 was added. The mixture was then heated at reflux for 16 hours. Excess POCl3 was removed in vacuum, and the residue was purified by column chromatography to provide 78 (3.11 g, 76%). Mass spectrum (ESI+): m/z=233 [M+1].
2.26 g (53%) In ice-water; trichlorophosphate; b) 3.6 g (0.01 8 mol) of 8-chloro-1,2,3,4-tetrahydroquinazoline-2,4-dione were suspended in 16.8 ml (0.18 mol) of phosphorus oxychloride and boiled under reflux for 17 hrs. The reaction mixture was left to cool to room temperature and poured on to ice-water. The brown precipitate was extracted with dichloromethane, chromatographed over silica gel with dichloromethane as the eluent and recrystallized from diisopropyl ether. Yield: 2.26 g (53%) of 2,4,8-trichloro-quinazoline as yellow crystals; m.p. 155-156 C.
With N,N-dimethyl-aniline; trichlorophosphate; at 115℃; for 4h; Second Step: Step 2-2 of Scheme 2 A mixture of the product (VI)-B (700 mg, 3.56 mmol) of the first step, N,N-dimethylaniline (0.1 mL) and POCl3 (7 mL) was stirred at 115C for 4 hours. After cooling to room temperature, the reaction mixture was added to ice water (20 mL). The precipitated solid was collected by filtration, washed with water and then dried to obtain 414 mg of 2,4,8-trichloroquinazoline (VII)-B, which is a kind of the compound (VII) in Scheme 2. [Show Image] 1H-NMR (CD3OD) d (ppm): 8.31 (d, 1H, J = 8.1 Hz) 8.21 (d, 1H, J = 8.7 Hz), 7.78 (t, 1H, J = 8.1 Hz).
  • 2
  • [ 62484-22-4 ]
  • [ 62484-29-1 ]
YieldReaction ConditionsOperation in experiment
With N,N-dimethyl-aniline; trichlorophosphate; at 140℃; for 16h; Step C: 2A8-trichloroquinazoline [0145] 8-Chloroquinazoline-2,4-diol (step B, 15 g, 75.8 mmol) was added to POCl3 (70 mL, 763 mmol, 10 equiv.) in small portions. Dimethylaniline (3.7 g, 30.5 mmol, 0.4 equiv.) was added. The reaction mixture was stirred in 140 C for 16 hours. The mixture was cooled to room temperature, and added drop wise to ice-water (500 mL). The precipitate was collected and washed with ice-water. The solid was dissolved in DCM (500 mL), dried over MgS04, filtered, and concentrated to give the crude product, which was purified by silica column chromatography (petroleum ether: EtOAc = 7:1 ) to afford the title compound as a yellow solid which was characterized by LC MS. LC-MS: m/z (M+l ) = 233.
With N,N-dimethyl-aniline; trichlorophosphate; at 140℃; for 16h; 8-Chloroquinazoline-2,4-diol (step B, 15 g, 75.8 rnmol) was added to POC13 (70 mL, 763 mmol, 10 equiv.) in small portions. Dirnethylaniline (3.7 g, 30.5 rnmol, 0.4 equiv.) was added. The reaction mixture was stirred in 140C for 16 hours. The mixture was cooled to room temperature, and added drop wise to ice-water (500 mL). The precipitate was collected and washed with ice-water. The solid was dissolved in DCM (500 rnL), dried over MgSO4, filtered, and concentrated to give the crude product, which was purified by silica column chromatography (petroleum ether: EtOAc = 7:1) to afford the title compound as a yellow solid which was characterized by LC/MS. LC-MS: m/z (M+1) = 233.
With N,N-dimethyl-aniline; trichlorophosphate; at 140℃; for 16h; 8-Chloroquinazoline-2,4-diol (step B, 15 g, 75.8 mmol) was added to POCI3 (70 mL, 763 mmol, 10 equiv.) in small portions. Dimethylaniline (3.7 g, 30.5 mmol, 0.4 equiv.) was added. The reaction mixture was stirred in 140C for 16 hours. The mixture was cooled to room temperature, and added drop wise to ice-water (500 mL). The precipitate was collected and washed with ice-water. The solid was dissolved in DCM (500 mL), dried over MgS04, filtered, and concentrated to give the crude product, which was purified by silica column chromatography (petroleum ether: EtOAc = 7: 1) to afford the title compound as a yellow solid which was characterized by LC/MS. LC-MS: m/z (M+l) = 233.
 

Historical Records

Technical Information

Categories