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CAS No. : | 3621-81-6 | MDL No. : | MFCD09264312 |
Formula : | C7H3Cl2NO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | JOXBFDPBVQGJOJ-UHFFFAOYSA-N |
M.W : | 188.01 | Pubchem ID : | 10397578 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
76% | With triethylamine; In dichloromethane; at 20℃; for 1h; | A solution of Compound 6g (226 mg, 1 mmol) and Compound 9 (224 mg, 1.2 mmol) and TEA (200 mg, 2 mmol) in DCM (10 ml) was stirred at r.t. for 1 hr. The reaction was concentrated and purified by silica gel chromatography (elutingwith petroleum ether/EtOAc=100:1~6:1) to give compound 7a (350 mg, yield: 76%). 1H NMR (400MHz, CHLOROFORM-d) delta= 7.31 (d, J=2.0 Hz, 1H), 7.15 (d, J=8.6 Hz,1H), 6.97 (dd, J=2.0, 8.4 Hz, 1H), 4.06 (d, J=10.6 Hz, 1H), 3.81 (t, J=8.9 Hz, 1H),3.72 (dd, J=5.7, 10.6 Hz, 1H), 3.60 - 3.46 (m, 2H), 2.78 (t, J=12.3 Hz, 1H), 2.31 (qd,J=5.8, 11.9 Hz, 1H), 1.85 (d, J=11.9 Hz, 1H), 1.77 - 1.65 (m, 2H), 1.49 (s, 9H), 1.38-1.35 (m, 2H) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90.4% | 18.2 g of compound A1 was dissolved in 100 mL of DMF, 40 g of anhydrous potassium carbonate was added thereto with stirring, and the temperature was raised to 80 C, and the reaction was stirred for 1 hour, and the temperature was lowered to room temperature.Then 18.8 g of compound A2 was added in portions,The reaction was continued to warm to 80 C and the reaction was stirred for 1 hour and allowed to cool to room temperature.Dilute with 500 mL of water, adjust the pH to about 3 with hydrochloric acid, and precipitate a large amount of white solid.Filter by suction. The filter cake was dried to give 30.1 g of a white solid, Compound A3.The yield was 90.4%, and the HPLC purity was greater than 95%. |
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