3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With acetic acid; zinc for 4h; | 99% |
With sodium sulfide; zinc at 35 - 45℃; for 0.333333h; Temperature; | 90% |
2,3-dibromo-5-chloroaniline
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With hydrogenchloride; 2H(1+)*2H3N*Cl3Cu(2-) In acetic acid at 90℃; Rate constant; other solvent, other temp., other Cu(I) complex; |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With hydrogenchloride; tin |
benzenesulfonic acid
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: nitric acid; manganese(IV) oxide / 0.75 h / 35 °C / 15001.5 Torr 2: N-Bromosuccinimide / 30 °C 3: hydrogenchloride / water / 1 h / 95 °C / 18751.9 Torr 4: acetic acid / 0.75 h / 20 - 25 °C / 15001.5 - 18751.9 Torr 5: zinc; sodium sulfide / 0.33 h / 35 - 45 °C View Scheme |
p-nitrobenzenesulfonic acid
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: N-Bromosuccinimide / 30 °C 2: hydrogenchloride / water / 1 h / 95 °C / 18751.9 Torr 3: acetic acid / 0.75 h / 20 - 25 °C / 15001.5 - 18751.9 Torr 4: zinc; sodium sulfide / 0.33 h / 35 - 45 °C View Scheme |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: hydrogenchloride / water / 1 h / 95 °C / 18751.9 Torr 2: acetic acid / 0.75 h / 20 - 25 °C / 15001.5 - 18751.9 Torr 3: zinc; sodium sulfide / 0.33 h / 35 - 45 °C View Scheme |
potassium cyclopropyltrifluoroborate
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium tert-butylate In water; toluene at 90℃; for 16h; Inert atmosphere; | 92.4% |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With triethylamine; HATU In N,N-dimethyl-formamide at 0 - 20℃; for 12h; | 88.3% |
2-amino-6-methyl-4-chloropyrimidine
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water at 140℃; for 1.5h; Microwave irradiation; Sealed tube; | 87% |
3-bromo-5-chlorophenylamine
2-isopropenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In 1,4-dioxane; water at 130℃; for 3h; | 82% |
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In 1,4-dioxane; water at 100℃; for 12h; Inert atmosphere; | 51.1% |
3-bromo-5-chlorophenylamine
bis(pinacol)diborane
3-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In 1,4-dioxane at 110℃; for 5h; | 81.4% |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In 1,4-dioxane; water at 130℃; for 12h; Inert atmosphere; | 81% |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
Stage #1: 3-bromo-5-chlorophenylamine With hydrogenchloride; sodium nitrite In water at 0℃; Cooling with ice/salt; Stage #2: With copper(II) choride dihydrate; sulfur dioxide In water; acetic acid at 20℃; Cooling with ice/salt; | 78% |
Stage #1: 3-bromo-5-chlorophenylamine With hydrogenchloride; sodium nitrite In water at 5℃; Sandmeyer reaction; Stage #2: With sulfur dioxide; acetic acid; copper(l) chloride In water at 20℃; for 2h; Sandmeyer reaction; | |
Stage #1: 3-bromo-5-chlorophenylamine With hydrogenchloride; sodium nitrite In water at 0℃; for 0.666667h; Stage #2: With sulfur dioxide; acetic acid; copper(l) chloride In water at 0 - 20℃; for 2h; |
4-amino-6-chloro-2-methylpyrimidine
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water for 18h; Reflux; | 75% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Reflux; | 75% |
3-bromo-5-chlorophenylamine
2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In water at 100℃; for 12h; Inert atmosphere; | 54.2% |
3-bromo-5-chlorophenylamine
4-pyridylboronic acid
3-chloro-5-(pyridin-4-yl)aniline
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In 1,4-dioxane; water at 100℃; for 12h; Inert atmosphere; | 53.1% |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With trimethylaluminum In toluene at 0 - 110℃; for 3h; | 52.4% |
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In 1,4-dioxane; water at 110℃; for 12h; Inert atmosphere; | 50.4% |
3-bromo-5-chlorophenylamine
3-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Conditions | Yield |
---|---|
In ethyl acetate | 48% |
n-propanesulfonyl chloride
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With pyridine at 20℃; for 48h; | 48% |
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran at 40℃; for 12h; | 41.1% |
2,3-dihydro-2H-furan
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; triphenylphosphine In N,N-dimethyl-formamide at 110℃; for 12h; Inert atmosphere; | A 41.1% B 24.8% |
3-bromo-5-chlorophenylamine
2-methyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-propene
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In 1,4-dioxane; water at 120℃; for 12h; Inert atmosphere; | 41% |
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In N,N-dimethyl-formamide at 20 - 85℃; for 16h; Inert atmosphere; | 38.7% |
3-bromo-5-chlorophenylamine
Conditions | Yield |
---|---|
With N-chloro-succinimide In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere; | 34% |
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate In 1,4-dioxane; water at 100℃; for 22h; Inert atmosphere; | 24% |
3-bromo-5-chlorophenylamine
1-bromo-3-chloro-5-iodobenzene
Conditions | Yield |
---|---|
ueber die Diazoverbindung; |
3-bromo-5-chlorophenylamine
p-acetylaminobenzenesulfonyl chloride
Conditions | Yield |
---|---|
With pyridine; acetone Erwaermen des Reaktionsprodukts mit wss. Natronlauge; |
N-tert-butoxycarbonyl-L-phenylalanine
3-bromo-5-chlorophenylamine
(S)-tert-butyl 1-(3-bromo-5-chlorophenylamino)-1-oxo-3-phenylpropan-2-ylcarbamate
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide for 14h; |
morpholine
3-bromo-5-chlorophenylamine
3-chloro-5-morpholinoaniline
Conditions | Yield |
---|---|
With lithium hexamethyldisilazane; tris-(dibenzylideneacetone)dipalladium(0); 2-dicyclohexylphosphino-2,4,6-triisopropylbiphenyl In tetrahydrofuran at 65℃; for 2.5h; |
Conditions | Yield |
---|---|
With copper(l) iodide; 1-(5,6,7,8-tetrahydroquinolin-8-yl)ethan-1-one; caesium carbonate In N,N-dimethyl-formamide at 130℃; for 24h; Inert atmosphere; |
The IUPAC name of 3-Bromo-5-chloroaniline is 3-bromo-5-chloroaniline . The CAS registry number is 96558-78-0. It is also named as Benzenamine, 3-bromo-5-chloro- ; 3-Bromo-5-chlorophenylamine . It is pharmaceutical intermediates and can be used in pharmaceutical synthesis. People can use the following data to convert to the molecule structure. SMILES: c1c(cc(cc1Cl)Br)N; InChI: InChI=1/C6H5BrClN/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2; InChIKey:YYBRLVWWPRAQDX-UHFFFAOYAR; Std. InChI:
InChI=1S/C6H5BrClN/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2; Std. InChIKey: YYBRLVWWPRAQDX-UHFFFAOYSA-N.
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