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CAS No. : | 40928-13-0 | MDL No. : | MFCD00090431 |
Formula : | C8H4ClNO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | QRUPDIJQZCABTC-UHFFFAOYSA-N |
M.W : | 197.58 | Pubchem ID : | 329105 |
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 |
---|---|---|
In tetrahydrofuran; | PREPARATION 11 A mixture of 7-chloro-2H-3,1-benzoxazine-2,4(1H)dione (18.4 g) and <strong>[112734-22-2]4-bromo-2-fluorobenzylamine</strong> (26 g) in tetrahydrofuran (200 ml) was refluxed for 15 minutes. After cooling, tetrahydrofuran was evaporated to give a residue. Recrystallization from isopropyl ether gave 2-amino-N-(4-bromo-2-fluorobenzyl)-4-chlorobenzamide (26.6 g). mp: 119.5 C. IR (Nujol): 3460, 3350, 3260, 1625, 1605 cm-1. NMR (DMSO-d6, delta): 4.4 (2H, d, J=5.6 Hz), 6.5-6.8 (4H, m), 7.3-7.6 (4H, m), 8.8 (1H, t, J=5.6 Hz). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With ammonium carbonate; In 1,4-dioxane; at 60℃; | General procedure: Compound 13 was prepared according to the procedurepreviously reported.37 A suspension of isatoic anhydride 12 (40mmol), ammonium carbonate (160 mmol), and 1,4-dioxane(150 mL) was heated at 60 C. After being stirred for 5-8 h,the reaction mixture was cooled to room temperature andevaporated under reduced pressure, and then water (200 mL)was added to the residue, which was extracted three times withEtOAc (300 mL). The organic layer was washed with brine(100 mL), dried over anhydrous Na2SO4, filtered, andconcentrated to afford compound 13 in yields of 80-85%. | |
With ammonium carbonate; In 1,4-dioxane; at 60℃; for 8h; | General procedure: A suspension of isatoic anhydride (35 mmol), ammonium carbonate (140 mmol), and 1,4-dioxane (150 mL) was heated at 60 C. After stirring for 8 h, the reaction mixture was cooled to room temperature and evaporated underreduced pressure, and then water (200 mL) was added to the residue, which was extracted with DCM (80 mL × 3). The organic layerwas dried over anhydrous Na2SO4, and concentrated to give compound 3 in yield of 84%. | |
With ammonium carbonate; In 1,4-dioxane; at 60℃; for 8h; | General procedure: A suspension of substituted isatoic anhydride (35 mmol), ammonium carbonate (140 mmol), and 1,4-dioxane (150 mL) was heated at 60 C. After stirring for 8 h, the reaction mixture was cooled to room temperature and evaporated under reduced pressure, and then water (200 mL) was added to the residue, which was extracted with CH2Cl2 (380 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to give compounds 9 in yields of 63-94%. |
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