Home Cart Sign in  
Chemical Structure| 6845-81-4 Chemical Structure| 6845-81-4

Structure of 6845-81-4

Chemical Structure| 6845-81-4

*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 [ 6845-81-4 ]

CAS No. :6845-81-4
Formula : C9H7ClO3
M.W : 198.60
SMILES Code : O=C(Cl)CC1=CC=C(OCO2)C2=C1
MDL No. :MFCD03424722

Safety of [ 6845-81-4 ]

Application In Synthesis of [ 6845-81-4 ]

* 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 [ 6845-81-4 ]

[ 6845-81-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 126674-77-9 ]
  • [ 6845-81-4 ]
  • [ 1272533-66-0 ]
YieldReaction ConditionsOperation in experiment
80% In pyridine; dichloromethane; at 120℃; for 0.0833333h;Microwave irradiation; 2-(2-benzo[1 ,31dioxol-5-yl-acetylamino)-4,6-difluoro-benzoic acid (V) To a solution of commercially available benzo[1 ,3]dioxol-5-yl-acetyl chloride (3.70 g, 18.70 mmol) in anhydrous dichloromethane (20 mL) was added <strong>[126674-77-9]2-amino-4,6-difluoro-benzoic acid</strong> (2.20 g, 12.5 mmol). After the addition of pyridine (5 mL), the mixture was heated under microwave condition at 120C for 5 minutes. The solvent was evaporated and the residue was diluted with 2 N HCI solution to induce the precipitation of a brown solid which was filtered, washed with water and dried under vacuum at 50C, to afford the title compound (3.34 g, 80% yield).1 H-NMR (400 MHz), delta (ppm, DMSO-cie): 12.21 (bs, 1 H), 10.65 (bs, 1 H), 7.93 (m, 1 H), 7.07 (m, 1 H), 6.90 (d, 1 H), 6.88 (d, 1 H), 6.80 (dd, 1 H), 5.99 (s, 2 H), 3.66 (bs, 2 H).
80% With pyridine; In dichloromethane; at 120℃; for 0.0833333h;Microwave irradiation; Step 22-(2-benzo[1,3]dioxol-5-yl-acetylamino)-4,6-difluoro-benzoic acid (V)To a solution of commercially available benzo[1,3]dioxol-5-yl-acetyl chloride (3.70 g, 18.70 mmol) in anhydrous dichloromethane (20 mL) was added <strong>[126674-77-9]2-amino-4,6-difluoro-benzoic acid</strong> (2.20 g, 12.5 mmol). After the addition of pyridine (5 mL), the mixture was heated under microwave condition at 120 C. for 5 minutes. The solvent was evaporated and the residue was diluted with 2 N HCl solution to induce the precipitation of a brown solid which was filtered, washed with water and dried under vacuum at 50 C., to afford the title compound (3.34 g, 80% yield).1H-NMR (400 MHz), delta (ppm, DMSO-d6): 12.21 (bs, 1H), 10.65 (bs, 1H), 7.93 (m, 1H), 7.07 (m, 1H), 6.90 (d, 1H), 6.88 (d, 1H), 6.80 (dd, 1H), 5.99 (s, 2H), 3.66 (bs, 2H).
With pyridine; In dichloromethane; at 120℃; for 0.0833333h;Microwave irradiation; General procedure: To a solution of acyl chlorides (18.70 mmol) in anhydrous dichloromethane (20 mL) was added 2-amino-benzoic acid derivatives 4 (12.5 mmol). After the addition of pyridine (5 mL), the mixture was heated under microwave condition at 120 C for 5 min. The solvent was evaporated and the residue was diluted with 2 N HCl solution to induce the precipitation of a brown solid which was filtered, washed with water and dried under vacuum at 50 C, to afford the 2-acylamine-benzoic acids 5. A stirred solution of compounds 5 (25 mmol) in acetic anhydride (50 mL) was refluxed for 10 min. The solvent was removed in vacuum and the residue was taken up in diethyl ether, to provide after filtration and drying the title benzoxazin-4-ones 6. A solution of benzoxazin-4-ones 6 (20.2 mmol) and aminoguanidine hydrogencarbonate (20.2 mmol) in pyridine (25 mL) was heated under microwave condition at 180 C for 30 min. The reaction was cooled at room temperature and diluted with methanol/water 1:1 to induce the precipitation of a brown solid which was washed with a mixture MeOH/H2O 8:2, to afford the desired compounds
 

Historical Records

Technical Information

Categories