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CAS No.: | 4943-85-5 |
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Name: | 2-AMINO-N-(2-METHYLPHENYL)BENZAMIDE |
Article Data: | 31 |
Molecular Structure: | |
Formula: | C14H14N2O |
Molecular Weight: | 226.278 |
Synonyms: | Anthranilsaeure-o-toluidid;2-Aminobenzoesaeure-2'-methylanilid;2-Amino-benzoesaeure-o-toluidid;anthranilic acid o-toluidide; |
PSA: | 55.12000 |
LogP: | 3.48370 |
Conditions | Yield |
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With tetrahydroxydiboron; 5%-palladium/activated carbon; water In acetonitrile at 50℃; for 24h; | 99% |
With tetrahydroxydiboron; palladium on activated charcoal; water In acetonitrile at 50℃; for 24h; Inert atmosphere; | 99% |
With hydrogen; palladium on activated charcoal In ethyl acetate under 750.075 Torr; | 87% |
2-methylchlorobenzene
anthranilic acid amide
A
2-amino-N-(2-methylphenyl)benzamide
B
2-(2-methylphenylamino)benzamide
Conditions | Yield |
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With palladium diacetate; potassium carbonate; XPhos In tert-butyl alcohol at 110℃; for 17h; | A 10% B 87% |
Conditions | Yield |
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With aqueous extract of mesocarp of fruit of Balanites roxburghii plant at 60℃; for 0.333333h; | 83% |
In ethanol for 20h; Reflux; | 67% |
Conditions | Yield |
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In diethyl ether at 0 - 10℃; for 0.5h; | 81.39% |
Conditions | Yield |
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In ethyl acetate at 90℃; for 18h; | 50% |
methaqualone
A
2-Acetamidobenzoesaeure-2'-methylanilid
B
2-amino-N-(2-methylphenyl)benzamide
C
o-toluidine
Conditions | Yield |
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With sodium hydroxide for 7h; Heating; hydrolysis; |
Conditions | Yield |
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Multi-step reaction with 2 steps 1: 63 percent / aq. K2CO3 / tetrahydrofuran / 12 h / Heating 2: 51 percent / H2 / 5percent Pd/C / 3 h / 2327.2 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 63 percent / aq. K2CO3 / tetrahydrofuran / 12 h / Heating 2: 51 percent / H2 / 5percent Pd/C / 3 h / 2327.2 Torr View Scheme |
2-methylchlorobenzene
anthranilic acid amide
A
2-amino-N-(2-methylphenyl)benzamide
B
2-(2-methylphenylamino)benzamide
Conditions | Yield |
---|---|
With potassium carbonate; tris-(dibenzylideneacetone)dipalladium(0) In hexane | A 98 mg (87%) B n/a |
Conditions | Yield |
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Multi-step reaction with 2 steps 1: thionyl chloride / 4.5 h / 80 °C 2: diethyl ether / 0.5 h / 0 - 10 °C View Scheme |