5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
Stage #1: C11H13N3O2S With hydroxylamine hydrochloride; potassium carbonate In water at 85℃; for 2h; Stage #2: With hydrogenchloride In water for 1h; | 80% |
Conditions | Yield |
---|---|
Stage #1: 3-hydroxybutanenitrile With hydroxylamine hydrochloride; potassium carbonate In water at 20 - 60℃; for 3h; Stage #2: With iron(III) chloride In toluene Reagent/catalyst; Temperature; Reflux; | 77% |
2-(5-methyl-1,2-oxazol-3-yl)-1H-isoindole-1,3(2H)-dione
5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 3h; Heating; | 75.1% |
C4H4N2O2S
cyclohexa-1,3-diene
A
5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 22h; hetero-Diels-Alder reaction; | A n/a B n/a C 64% |
(5-methyl-isoxazol-3-yl)-carbamic acid benzyl ester
5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
With sodium hydroxide |
(5-methyl-isoxazol-3-yl)-carbamic acid ethyl ester
5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
(i) Br2, MeOH, (ii) aq. NaOH, NH2CONHOH; Multistep reaction; |
(Z)-4-(5-Methyl-isoxazol-3-ylamino)-pent-3-en-2-one
5-methylisoxazol-3-ylamine
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol for 3h; Heating; Yield given; |
Conditions | Yield |
---|---|
With sodium hypochlorite; borate buffer at 25℃; pH=9; Kinetics; Further Variations:; pH-values; Reagents; Solvents; |
sulfamethoxazole
A
5-methylisoxazol-3-ylamine
D
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
Conditions | Yield |
---|---|
With hydrogenchloride; water; sodium chloride; sodium hydroxide pH=9.5; Catalytic behavior; Mechanism; Kinetics; pH-value; Reagent/catalyst; Inert atmosphere; |
sulfamethoxazole
A
5-methylisoxazol-3-ylamine
B
benzenesulfonamide
C
1,2,4-Trihydroxybenzene
D
N-((4-aminophenyl)sulfonyl)carbamimidic acid
E
3-hydroxybenzenesulfonamide
O
4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide
P
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
Q
phenol
Conditions | Yield |
---|---|
With AgBr-BaMoO4 composite photocatalyst In water for 1.25h; Kinetics; Reagent/catalyst; UV-irradiation; |
sulfamethoxazole
A
5-methylisoxazol-3-ylamine
B
5-methyl-3-nitrosoisoxazole
Conditions | Yield |
---|---|
With sodium sulfate In water pH=7; Kinetics; pH-value; Reagent/catalyst; Electrochemical reaction; |
N1-acetylsulfamethoxazole
A
5-methylisoxazol-3-ylamine
B
5-methyl-3-nitrosoisoxazole
C
N-acetylsulfanilic acid
D
nitroso derivative of sulfamethoxazole
E
Benzenesulfinic acid
F
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
Conditions | Yield |
---|---|
With sodium sulfate In water pH=7; Kinetics; pH-value; Reagent/catalyst; Electrochemical reaction; |
sulfamethoxazole
A
5-methylisoxazol-3-ylamine
B
3-nitro-5-methylisoxazole
C
5-methyl-3-nitrosoisoxazole
Conditions | Yield |
---|---|
With iron(III) sulfate; sodium hydrogensulfite at 25℃; pH=4; Kinetics; pH-value; |
sulfamethoxazole
A
5-methylisoxazole
B
5-methylisoxazol-3-ylamine
C
1-hydroxy-2-aminobenzene-5-sulfonic acid
E
4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide
G
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
Conditions | Yield |
---|---|
Stage #1: sulfamethoxazole With 0D/1D 50 wt.% AgI/MoO3 Z-scheme heterojunction composite In water for 0.5h; Darkness; Sonication; Stage #2: In water pH=3.92; Kinetics; Catalytic behavior; Reagent/catalyst; Irradiation; |
5-methylisoxazol-3-ylamine
5-chlorosalicyclaldehyde
3-(2-hydroxy-8-chlorobenzylideneamino)-5-methylisoxazole
Conditions | Yield |
---|---|
Reflux; | 100% |
In ethanol for 2h; Reflux; | 88% |
In ethanol Heating; |
5-methylisoxazol-3-ylamine
5-bromosalicyclaldehyde
4-bromo-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
Conditions | Yield |
---|---|
Reflux; | 100% |
In ethanol for 2h; Reflux; | 95% |
In ethanol Heating; |
5-methylisoxazol-3-ylamine
piperonal
[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
Conditions | Yield |
---|---|
Heating; | 100% |
In ethanol; chloroform |
5-methylisoxazol-3-ylamine
4-methyl-benzaldehyde
(5-Methyl-isoxazol-3-yl)-[1-p-tolyl-meth-(E)-ylidene]-amine
Conditions | Yield |
---|---|
Heating; | 100% |
With 1-methylimidazolium tetrafluoroborate at 30℃; for 0.25h; | |
In ethanol; chloroform |
5-methylisoxazol-3-ylamine
4-chlorobenzaldehyde
N-(4-chlorobenzylidene)-5-methylisoxazol-3-amine
Conditions | Yield |
---|---|
Heating; | 100% |
With 1-methylimidazolium tetrafluoroborate at 30℃; | |
In ethanol; chloroform | |
In ethanol Reflux; |
5-methylisoxazol-3-ylamine
2-chloro-benzaldehyde
[1-(2-Chloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
Conditions | Yield |
---|---|
Heating; | 100% |
With trimethylsilyl acetate; zinc(II) chloride In N,N-dimethyl-formamide at 100℃; for 8h; |
5-methylisoxazol-3-ylamine
3-nitro-benzaldehyde
(5-Methyl-isoxazol-3-yl)-[1-(3-nitro-phenyl)-meth-(E)-ylidene]-amine
Conditions | Yield |
---|---|
Heating; | 100% |
In ethanol; chloroform |
5-methylisoxazol-3-ylamine
4-nitrobenzaldehdye
(5-Methyl-isoxazol-3-yl)-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-amine
Conditions | Yield |
---|---|
Heating; | 100% |
In ethanol; chloroform | |
With acetic acid In 1,2-dichloro-ethane at 60℃; for 1.5h; | |
With tert-butylisonitrile; phenylpropyolic acid In methanol at 20℃; for 24h; |
5-methylisoxazol-3-ylamine
benzaldehyde
N-benzylidene-5-methylisoxazol-3-amine
Conditions | Yield |
---|---|
Heating; | 100% |
With 1-methylimidazolium tetrafluoroborate at 30℃; for 0.25h; | |
In ethanol; chloroform | |
With acetic acid In 1,2-dichloro-ethane at 60℃; for 1.5h; | |
With magnesium sulfate In ethanol at 20℃; |
5-methylisoxazol-3-ylamine
4-methoxy-benzaldehyde
[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
Conditions | Yield |
---|---|
Heating; | 100% |
With piperidine In ethanol for 0.166667h; Reflux; | 76% |
With 1-methylimidazolium tetrafluoroborate at 30℃; | |
In ethanol; chloroform |
5-methylisoxazol-3-ylamine
2,4-dichlorobenzaldeyhde
[1-(2,4-Dichloro-phenyl)-meth-(E)-ylidene]-(5-methyl-isoxazol-3-yl)-amine
Conditions | Yield |
---|---|
Heating; | 100% |
In ethanol; chloroform |
5-methylisoxazol-3-ylamine
2-hydroxy-5-methoxybenzaldehyde
4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
Conditions | Yield |
---|---|
Reflux; | 100% |
In ethanol for 2h; Reflux; | 90% |
5-methylisoxazol-3-ylamine
2-hydroxy-5-methylbenzaldehyde
4-methyl-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
Conditions | Yield |
---|---|
Reflux; | 100% |
In ethanol for 2h; Reflux; | 90% |
5-methylisoxazol-3-ylamine
salicylaldehyde
2-((5-methylisoxazol-3-ylimino)methyl)phenol
Conditions | Yield |
---|---|
Reflux; | 100% |
In ethanol for 2h; Reflux; | 95% |
In methanol Reflux; | 82% |
Conditions | Yield |
---|---|
Reflux; | 100% |
Conditions | Yield |
---|---|
Reflux; | 100% |
Conditions | Yield |
---|---|
[{Me2Si(C5Me4)(NPh)}Y(CH2SiMe3)(thf)2] In tetrahydrofuran at 20℃; for 1h; | 99% |
5-methylisoxazol-3-ylamine
mercaptoacetic acid
4-cyanobenzaldehyde
4-(3-(5-methylisoxazol-3-yl)-4-oxothiazolidin-2-yl)benzonitrile
Conditions | Yield |
---|---|
In toluene Reflux; Dean-Stark; | 98.7% |
5-methylisoxazol-3-ylamine
2,7-Dihydroxynaphthalene
4-fluorobenzaldehyde
C21H17FN2O3
Conditions | Yield |
---|---|
at 80℃; for 0.5h; Neat (no solvent); | 98% |
5-methylisoxazol-3-ylamine
(1,1,1-trifluoro-2-(trifluoromethyl)-but-2-yl)isocyanate
1-[1,1-bis(trifluoromethyl)propyl]-3-(5-methylisoxazol-3-yl)urea
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 4h; | 98% |
5-methylisoxazol-3-ylamine
4-Nitrobenzenesulfonyl chloride
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide
Conditions | Yield |
---|---|
With pyridine at 20℃; for 5h; | 97% |
95% | |
With pyridine at 0℃; for 2h; Inert atmosphere; | 90% |
5-methylisoxazol-3-ylamine
C12H12ClN3O
1-(3,4-dimethylphenyl)-5-methyl-N-(5-methylisoxazol-3-yl)-1H-1,2,3-triazole-4-carboxamide
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 70℃; | 97% |
Conditions | Yield |
---|---|
With [2-(di-tert-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-((2-aminoethyl)phenyl)]palladium(II) chloride; sodium t-butanolate; tert-butyl XPhos In tert-butyl alcohol at 20℃; for 2h; Inert atmosphere; | 97% |
5-methylisoxazol-3-ylamine
2,7-Dihydroxynaphthalene
4-nitrobenzaldehdye
1-[(5-methylisoxazol-3-ylamino)(4-nitrophenyl)methyl]naphthalene-2,7-diol
Conditions | Yield |
---|---|
at 80℃; for 0.5h; Neat (no solvent); | 97% |
5-methylisoxazol-3-ylamine
1H-indol-2-ylcarboxaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol at 30℃; for 0.2h; Temperature; Sonication; | 97% |
Conditions | Yield |
---|---|
With acetic acid In methanol at 30℃; for 0.2h; Temperature; Sonication; | 97% |
5-methylisoxazol-3-ylamine
2,6-difluorobenzaldehyde
mercaptoacetic acid
2-(2,6-difluorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one
Conditions | Yield |
---|---|
In toluene Reflux; | 96.7% |
5-methylisoxazol-3-ylamine
2,6-dichlorobenzaldehyde
mercaptoacetic acid
2-(2,6-dichlorophenyl)-3-(5-methylisoxazol-3-yl)thiazolidin-4-one
Conditions | Yield |
---|---|
In toluene Reflux; | 96.5% |
Conditions | Yield |
---|---|
for 1.5h; Heating; | 96% |
5-methylisoxazol-3-ylamine
ethyl (ethoxymethylene)cyanoacetate
ethyl 2-cyano-3-(5-methylisoxazol-3-ylamino)acrylate
Conditions | Yield |
---|---|
In ethanol for 1.5h; Reflux; | 96% |
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