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inquiryProduct description: Product name 2,3,5-Trichloropyridine CAS number 16063-70-0 Assay ≥99% Appearance Yellowish to off-white powder Capacity 200mt/year Application Pharmaceut
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inquiryAbout Product Details Mol File: 16063-70-0.mol
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inquiryChemical Name: 2,3,5-Trichloropyridine CAS No.:16063-70-0 Appearance: white powder Assay:99% Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kg per bag or 25kg per drum Application:Animal Pharmac
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inquiry2,3,5,6-tetrachloropyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen; potassium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene; water at 60℃; under 4500.45 Torr; for 6h; Reagent/catalyst; Solvent; Pressure; Autoclave; | 99.1% |
With sodium hydroxide In benzene |
2,3,4,5,6-pentachloropyridine
A
2,3,6-trichloropyridine
B
2,3,5-trichloropyridine
C
2,3,5,6-tetrachloropyridine
Conditions | Yield |
---|---|
With ammonium chloride; dimethyl methane phosphonate; zinc In water at 85 - 90℃; Product distribution; other ammonium salts; other methylphosphonates/phosphates; | A 0.9% B 1% C 97.6% |
2,3,4,5-tetrachloro-pyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With tetramethylammonium methylphosphonic acid methyl ester; dimethyl methane phosphonate; zinc In water at 85℃; other ammonium salts; other methylphosphonates;other solvent(s). Object of study: selectivity of reaction; | 96.4% |
With ammonium chloride; zinc In methanol; water at 72℃; for 2h; Solvent; Temperature; | 90% |
With pyridine; 5%-palladium/activated carbon; hydrogen In methanol; water at 50℃; under 3750.38 Torr; Reagent/catalyst; Temperature; Pressure; | 86.2% |
With tetramethylammonium methylphosphonic acid methyl ester; dimethyl methane phosphonate; zinc In water at 85℃; for 1h; Yield given; | |
With ammonium chloride; zinc In methanol; water at 70 - 80℃; Temperature; Solvent; Large scale; | 1.4 kg |
3,5,6-trichloro-2-hydrazinopyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
95% | |
With sodium hypochlorite; sodium hydroxide In water at 70 - 75℃; for 1h; Green chemistry; | 95% |
93% |
2,4,4-trichloro-4-formylbutyronitrile
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With hydrogenchloride; phosphorus pentachloride In N,N-dimethyl-formamide at 60 - 100℃; for 1h; | 89% |
With hydrogenchloride at 180℃; for 2h; | 85% |
With hydrogenchloride at 80℃; for 3h; | 82.1% |
3,5-Dichloro-2-pyridinol
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With trichlorophosphate at 190℃; for 3h; in sealed tube; | 87% |
2,2,4'-trichloro-5-oxopentanonitrile
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With hydrogenchloride; trichlorophosphate In N,N-dimethyl-formamide at 115℃; for 0.333333h; | 79% |
With trichlorophosphate In benzene at 190℃; for 1h; in autoclave; | 76% |
Multi-step reaction with 2 steps 1: 91 percent / dry HCl / dimethylformamide / 0.25 h / 110 °C 2: 87 percent / POCl3 / 3 h / 190 °C / in sealed tube View Scheme | |
Multi-step reaction with 3 steps 1: 90 percent / dry HCl / dibutyl ether / 1 h / 90 °C 2: 95 percent / triethylamine / benzene / 4 h / Heating 3: 87 percent / POCl3 / 3 h / 190 °C / in sealed tube View Scheme |
2,3,4,5,6-pentachloropyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; sodium hydroxide; zinc In toluene at 50℃; for 6h; Green chemistry; | 73% |
With ammonium hydroxide In toluene | |
With sodium hydroxide; zinc In benzene | |
With sodium hypochlorite; sodium hydrogencarbonate; hydrazine In propylene glycol dimethyl ether; water |
Conditions | Yield |
---|---|
copper(l) chloride In acetonitrile at 190℃; for 0.5h; | 65% |
copper(l) chloride In acetonitrile at 190℃; for 0.5h; | 65% |
With [bmim]BF4; copper(l) chloride In acetonitrile at 120℃; | 41% |
In acetonitrile at 105 - 190℃; Product distribution; various inorg. catalyst, various yield; | |
copper(l) chloride In acetonitrile at 120 - 175℃; for 19h; |
Conditions | Yield |
---|---|
With chlorine In cyclohexane at 75℃; for 1h; | A 9% B 62% C 4.5% |
3,5-dichloropyridine-2-carboxylic acid
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With tert-butylhypochlorite; dichloromethane; oxygen; sodium hydrogencarbonate at 60℃; for 20h; Green chemistry; | 42% |
pyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With hydrogenchloride; chlorine at 115 - 120℃; | |
With phosphorus pentachloride at 210 - 220℃; |
phosgene
3,5-dichloro-1-methyl-1H-pyridin-2-one
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With toluene at 150℃; |
Conditions | Yield |
---|---|
With copper(I) chloride; trichlorophosphate 1. 5 h, 90 deg C, benzene, autoclave; 2. 30 min, 180 deg C.; Yield given. Multistep reaction; |
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With phosphorus pentachloride; trichlorophosphate at 180℃; im Rohr; |
3,5-dichloro-1-methyl-1H-pyridin-2-one
phosphorus pentachloride
trichlorophosphate
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
at 180℃; |
Conditions | Yield |
---|---|
With phosphorus pentachloride at 200℃; |
3,5-dichloropyridin-2-amine
A
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With hydrogenchloride; potassium nitrite |
hydrogenchloride
3,5-dichloropyridin-2-amine
A
2,3,5-trichloropyridine
2-(trichloromethyl)-3,5-dichloropyridine
A
tetrachloromethane
B
2,3,5-trichloropyridine
C
2,3,5-trichloro-6-(trichloromethyl)pyridine
Conditions | Yield |
---|---|
With chlorine at 200℃; Title compound not separated from byproducts; | |
With chlorine at 200℃; Rate constant; |
2-hydroxy-3,3,5-trichloro-3,4-dihydropyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 95 percent / triethylamine / benzene / 4 h / Heating 2: 87 percent / POCl3 / 3 h / 190 °C / in sealed tube View Scheme |
2-aminopyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: alcohol; chlorine 2: alcohol; chlorine 3: potassium nitrite; hydrochloric acid View Scheme | |
Multi-step reaction with 2 steps 1: alcohol; chlorine 2: potassium nitrite; hydrochloric acid View Scheme |
5-chloro-2-pyridylamine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: alcohol; chlorine 2: potassium nitrite; hydrochloric acid View Scheme |
2,3,5,6-tetrachloropyridine
A
2,3,5-trichloropyridine
B
3,5-dichloropyridine
Conditions | Yield |
---|---|
With ammonium chloride; zinc In 1,4-dioxane; water at 90 - 92℃; for 12h; Product distribution / selectivity; | A 7.7 %Chromat. B 77.8 %Chromat. |
3,5-dichloropyridin-2-amine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With sodium nitrite In hydrogenchloride; hexane; water | |
With hydrogenchloride; sodium nitrite In water at -20 - 20℃; for 4h; |
Conditions | Yield |
---|---|
In acetonitrile | 11.1 g (61% theory) |
3-Methoxypropionitrile
chloral
acrylonitrile
2,3,5-trichloropyridine
ammonium hydroxide
2,3,4,5,6-pentachloropyridine
1-methoxy-2-propanol
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
In water; toluene |
2,3,5-trichloro-4-hydrazino-pyridine
2,3,5-trichloropyridine
Conditions | Yield |
---|---|
With sodium hypochlorite In tetrahydrofuran |
2,3,5-trichloropyridine
propargyl alcohol
Conditions | Yield |
---|---|
Stage #1: propargyl alcohol With sodium hydride In tetrahydrofuran at 0 - 45℃; Stage #2: 2,3,5-trichloropyridine In tetrahydrofuran at 20 - 45℃; for 24h; | 100% |
2,3,5-trichloropyridine
2-amino-benzenethiol
3-chloro-1-azaphenothiazine
Conditions | Yield |
---|---|
With potassium hydroxide In water; N,N-dimethyl-formamide for 4h; Reflux; | 99.7% |
2,3,5-trichloropyridine
3,5-dichloro-2-bromopyridine
Conditions | Yield |
---|---|
With trimethylsilyl bromide In propiononitrile at 100℃; for 14h; | 99% |
With hydrogen bromide; propionic acid In water at 80℃; Reagent/catalyst; Solvent; | 96.8% |
2,3,5-trichloropyridine
(3,5-dichloro-2-pyridyl)hydrazine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol at 80℃; for 24h; | 96% |
With hydrazine hydrate | 95% |
With hydrazine hydrate In ethanol at 80 - 90℃; | 94.5% |
2,3,5-trichloropyridine
5-chloro-2,3-difluoropyridine
Conditions | Yield |
---|---|
With potassium fluoride; C6H10BNO4 In dimethyl sulfoxide at 60℃; for 5h; Solvent; Temperature; | 95% |
With potassium fluoride; 18-crown-6 ether; potassium carbonate; cesium fluoride In sulfolane; dimethyl sulfoxide at 120 - 200℃; for 3h; | 90% |
Multi-step reaction with 2 steps 1: 36.1 percent / KF; CsF; K2CO3 / [Bmim]BF4 / 10 h / 200 °C 2: 68.8 percent / CsF; K2CO3; [Bmim]BF4 / 8 h / 100 - 110 °C / 200 Torr View Scheme |
2,3,5-trichloropyridine
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With potassium carbonate; palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,2-dimethoxyethane at 85℃; for 2.5h; | 94.7% |
2,3,5-trichloropyridine
2-methyl-7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2H-indazole
7-(3,5-dichloro-pyridin-2-yl)-2-methyl-2H-indazole
Conditions | Yield |
---|---|
With potassium phosphate; tetrakis(triphenylphosphine) palladium(0) In DMF (N,N-dimethyl-formamide); water at 65℃; for 16h; | 93% |
2,3,5-trichloropyridine
p-cresol
2-(4-Methylphenoxy)-3,5-dichlorpyridin
Conditions | Yield |
---|---|
With copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; caesium carbonate In dimethyl sulfoxide at 110℃; for 24h; Inert atmosphere; regioselective reaction; | 93% |
2,3,5-trichloropyridine
4-Chlorophenylboronic acid
3,5-dichloro-2-(4-chlorophenyl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 91% |
2,3,5-trichloropyridine
4-methylphenylboronic acid
3,5-dichloro-2-p-tolylpyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 90% |
2,3,5-trichloropyridine
(RS)-2-(4-hydroxyphenoxy)propionic acid
D-2-[4-(3,5-dichloro-pyridin-2-yloxy)-phenoxy]-propionic acid
Conditions | Yield |
---|---|
With potassium carbonate at 75℃; for 4.5h; Reagent/catalyst; Temperature; | 90% |
Conditions | Yield |
---|---|
With potassium fluoride; tetrakis(triphenylphosphine) palladium(0) In toluene at 100℃; for 5h; | 90% |
With potassium fluoride; tetrakis(triphenylphosphine) palladium(0) In toluene at 100℃; for 5h; | 90% |
2,3,5-trichloropyridine
2,3,5-trichloro-4-iodopyridine
Conditions | Yield |
---|---|
With iodine; lithium diisopropyl amide In tetrahydrofuran; hexane at -75℃; | 89% |
Stage #1: 2,3,5-trichloropyridine With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: With iodine In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; | 75% |
2,3,5-trichloropyridine
4-fluoroboronic acid
3,5-dichloro-2-(4-fluorophenyl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 89% |
2,3,5-trichloropyridine
1-Naphthylboronic acid
3,5-dichloro-2-(naphthalen-1-yl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 89% |
2,3,5-trichloropyridine
phenylboronic acid
3,5-dichloro-2-phenylpyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 89% |
With palladium diacetate; potassium carbonate; triphenylphosphine In methanol; acetonitrile at 50℃; for 24h; Suzuki Coupling; Inert atmosphere; regioselective reaction; | 86% |
6-methoxypyridine-3-ol
2,3,5-trichloropyridine
5-(3,5-dichloro-pyridin-2-yloxy)-2-methoxy-pyridine
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide | 88% |
2,3,5-trichloropyridine
(meta-(trifluoromethyl)phenyl)boronic acid
3,5-dichloro-2-(3-(trifluoromethyl)phenyl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 88% |
2,3,5-trichloropyridine
3,5-dichloropyridine
Conditions | Yield |
---|---|
With acetic acid; zinc In water at 65 - 95℃; for 1 - 5.25h; Product distribution / selectivity; | 87.3% |
2,3,5-trichloropyridine
2-Methylphenylboronic acid
3,5-dichloro-2-o-tolylpyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 87% |
2,3,5-trichloropyridine
2-Fluoro-3,5-dichloropyridine
Conditions | Yield |
---|---|
With potassium fluoride In sulfolane at 180℃; for 20h; | 86% |
With potassium fluoride In sulfolane at 155 - 160℃; for 8h; Solvent; Temperature; |
Thien-3-ylboronic acid
2,3,5-trichloropyridine
3,5-dichloro-2-(thiophen-3-yl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 86% |
2,3,5-trichloropyridine
4-methoxyphenylboronic acid
3,5-dichloro-2-(4-methoxyphenyl)pyridine
Conditions | Yield |
---|---|
With palladium diacetate; sodium carbonate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki coupling; | 85% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 90℃; for 2h; methoxylation; | 83% |
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