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Items Standard Result Assay (Ursolic acid) 98%min 98.22% -----------------------------------------------------------------------------------------------------------
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inquiryProduct Description Product website: http://www.finerchem.com/pro01en/id/1940.html Product Name 6-Chloronicotinic acid CAS No. 5326-23-8
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inquiry6-Chloronicotinic acid Basic information Product Name: 6-Chloronicotinic acid Synonyms: RARECHEM AL BO 0729;TIMTEC-BB SBB004004;3-Pyridinecarboxylic acid, 6-chloro-;6-chloro-3-pyridineca
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inquiryProduct Name 6-Chloronicotinic acid CAS 5326-23-8 Molecular formula C6H4ClNO2 Molecular weight 157.55 EINECS 226-2
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A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Conditions | Yield |
---|---|
With hydrogenchloride pH=2; pH-value; | 98% |
With phosphorus pentachloride; trichlorophosphate at 120 - 130℃; |
2-chloro-5-(Trichloromethyl)-pyridine
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
In sulfuric acid | 94% |
With sulfuric acid; lithium acetate; water; silver; fluorosulphonic acid; acetic acid In methanol at 30 - 35℃; Solvent; Temperature; Electrolysis; | 84% |
2-chloro-5-methylpyridine
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate In chlorobenzene at 80℃; for 4h; Temperature; | 79.7% |
With potassium permanganate In water for 5h; Heating; | 60.1% |
Conditions | Yield |
---|---|
With formic acid; 1,3-bis-(diphenylphosphino)propane; nickel(II) acetate tetrahydrate; acetic anhydride In tetrahydrofuran at 100℃; for 24h; Schlenk technique; Inert atmosphere; Sealed tube; | 60% |
Conditions | Yield |
---|---|
With sodium hydroxide | A n/a B 54.2% |
A n/a B 53.8% | |
A n/a B 40.8% |
6-hydroxy-3-pyridinecarboxylic acid
phosphorus pentachloride
trichlorophosphate
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
at 120 - 130℃; eintragen des Reaktionsprodukts in Eiswasser; |
3-(1-methylpyrrolidin-2-yl)-6-chloropyridine
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
(+-)-Py 6-chloro-nicotine; |
1-(6-chloronicotinyl)-2-nitroiminoimidazoline
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With potassium permanganate In ethanol for 0.333333h; Oxidation; reflux; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 80 percent / 30percent H2O2 / acetic acid / 3 h / 90 °C 2: PCl5, POCl3 View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: KMnO4; H2O 2: aqueous HCl View Scheme |
6-chloro-3-pyridinecarboxylic acid ethyl ester
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With water; lithium hydroxide In tetrahydrofuran |
1-(6-chloronicotinyl)-2-nitroiminoimidazoline
A
2-pyrrolidinon
B
6-Chloro-3-pyridinecarboxylic acid
C
6-chloro-3-pyridinecarboxamide
D
6-chloronicotinylaldehyde
E
n-Amyl nitrite
F
1-nitroisobutane
G
1-[(6-chloro-3-pyridinyl)-methyl]-imidazolidin-2-one
Conditions | Yield |
---|---|
With phosphotungstic acid supported on mesoporous sieve MCM-41 In water for 14h; Irradiation; |
acetamiprid
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With Er doped Ti/SnO2-Sb electrode for 3h; Kinetics; Electrochemical reaction; |
6-Chloro-3-pyridinecarboxylic acid
6-iodo-nicotinic acid
Conditions | Yield |
---|---|
With sodium iodide In butanone at 110℃; for 12h; Inert atmosphere; | 100% |
With hydrogen iodide; sodium iodide for 24h; Heating; | 45% |
With butanone; potassium iodide |
6-Chloro-3-pyridinecarboxylic acid
6-Chloronicotinoyl chloride
Conditions | Yield |
---|---|
With thionyl chloride at 90℃; Inert atmosphere; | 100% |
With oxalyl dichloride at 63℃; for 20h; | 98% |
With phosphorus pentachloride; trichlorophosphate for 4h; Heating; | 95% |
6-Chloro-3-pyridinecarboxylic acid
methyl 2-amino-3-phenylpropanoate hydrochloride
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; Stirring overnight; | 100% |
6-Chloro-3-pyridinecarboxylic acid
azetidine hydrochloride
5-(azetidin-1-ylcarbonyl)-2-chloropyridine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In dichloromethane at 20℃; Inert atmosphere; | 100% |
6-Chloro-3-pyridinecarboxylic acid
1-(1-(6-chloronicotinoyl)piperidin-4-yl)-3-(4-(trifluoromethoxy)phenyl)urea
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; Inert atmosphere; | 100% |
6-Chloro-3-pyridinecarboxylic acid
chloro-trimethyl-silane
6-chloronicotinic acid trimethylsilyl ester
Conditions | Yield |
---|---|
With 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 78℃; for 3h; Inert atmosphere; | 100% |
4-((5S,9R)-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro-[4.4]nonan-9-yl)benzonitrile
6-Chloro-3-pyridinecarboxylic acid
BMS-688521
Conditions | Yield |
---|---|
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine In ISOPROPYLAMIDE for 3h; Heating / reflux; Stage #2: 4-((5S,9R)-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro-[4.4]nonan-9-yl)benzonitrile In ISOPROPYLAMIDE at 95℃; for 30h; Stage #3: With water In ISOPROPYLAMIDE at 0℃; Product distribution / selectivity; | 98% |
With N-ethyl-N,N-diisopropylamine In ISOPROPYLAMIDE at 110℃; for 30h; Product distribution / selectivity; | 54% |
6-Chloro-3-pyridinecarboxylic acid
4-methoxy-benzylamine
6-chloro-N-(4-methoxy-benzyl)-nicotinamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 3h; | 97% |
6-Chloro-3-pyridinecarboxylic acid
di-tert-butyl dicarbonate
tert-butyl 2-chloro-5-pyridinecarboxylate
Conditions | Yield |
---|---|
With dmap In tetrahydrofuran for 4.5h; Reflux; | 97% |
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With dmap In tetrahydrofuran for 3h; Reflux; Stage #2: di-tert-butyl dicarbonate In tetrahydrofuran for 3h; Reflux; | 94% |
With dmap In tetrahydrofuran at 62.5℃; for 5.6h; Product distribution / selectivity; | |
With dmap In tetrahydrofuran at 62.5℃; Large scale reaction; | |
With dmap In tetrahydrofuran at 70℃; for 1h; Large scale; |
6-Chloro-3-pyridinecarboxylic acid
tert-butylamine
N-tert-butyl-6-chloro-nicotinamide
Conditions | Yield |
---|---|
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With thionyl chloride Stage #2: tert-butylamine | 97% |
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With thionyl chloride for 2h; Heating; Stage #2: tert-butylamine In dichloromethane at 20℃; for 20h; Further stages.; | 88% |
6-Chloro-3-pyridinecarboxylic acid
3-fluorophenylboronic acid
6-(3-fluorophenyl)-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With potassium carbonate; tetrakis(triphenylphosphine) palladium(0); tetrabutylammomium bromide In water; toluene for 20h; Product distribution / selectivity; Heating / reflux; | 97% |
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; N,N-dimethyl-formamide at 90℃; Product distribution / selectivity; | |
Stage #1: 6-Chloro-3-pyridinecarboxylic acid; 3-fluorophenylboronic acid With tetrabutylammomium bromide; potassium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; toluene for 20h; Reflux; Stage #2: With hydrogenchloride In water; toluene pH=3; |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 97% |
6-Chloro-3-pyridinecarboxylic acid
oxalyl dichloride
2-chloro-1-(6-chloropyridin-3-yl)ethanone
Conditions | Yield |
---|---|
Stage #1: 6-Chloro-3-pyridinecarboxylic acid; oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide for 2.5h; Stage #2: With diazomethyl-trimethyl-silane In dichloromethane; N,N-dimethyl-formamide for 2h; | 97% |
6-Chloro-3-pyridinecarboxylic acid
6-hydrazinylnicotinic acid
Conditions | Yield |
---|---|
With hydrazine hydrate at 100℃; for 4h; Inert atmosphere; | 96% |
With hydrazine hydrate In ethanol Reflux; | 91% |
With hydrazine hydrate In water for 6h; Heating; | 90% |
6-Chloro-3-pyridinecarboxylic acid
N,O-dimethylhydroxylamine*hydrochloride
6-chloro-N-methoxy-N-methylpyridine-3-carboxamide
Conditions | Yield |
---|---|
96% | |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In acetonitrile at 20 - 60℃; | 93% |
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With oxalyl dichloride In tetrahydrofuran at 20℃; for 1h; Stage #2: N,O-dimethylhydroxylamine*hydrochloride With triethylamine In dichloromethane at 20℃; for 1h; | 73.8% |
diazomethane
6-Chloro-3-pyridinecarboxylic acid
6-Chloronicotinic acid methyl ester
Conditions | Yield |
---|---|
95% | |
In tetrahydrofuran |
6-Chloro-3-pyridinecarboxylic acid
diazomethyl-trimethyl-silane
6-Chloronicotinic acid methyl ester
Conditions | Yield |
---|---|
In methanol; diethyl ether; toluene at 0℃; for 0.75h; Inert atmosphere; | 95% |
In methanol; diethyl ether; toluene at 0℃; for 0.5h; Inert atmosphere; | 95% |
In methanol | |
In methanol; diethyl ether; toluene at 20℃; for 0.5h; |
6-Chloro-3-pyridinecarboxylic acid
6-chloronicotinic acid 1-oxide
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In chloroform at 45℃; for 24h; | 93% |
With dihydrogen peroxide; trifluoroacetic acid at 0 - 45℃; | 64% |
With dihydrogen peroxide; trifluoroacetic acid | |
Multi-step reaction with 3 steps 1.1: diethyl ether; toluene; methanol / 0.75 h / 0 °C / Inert atmosphere 2.1: dihydrogen peroxide; methyltrioxorhenium(VII) / water; ethanol / 24 h / 20 °C 3.1: sodium hydroxide / methanol / 1 h / Reflux 3.2: 0 °C / pH 4-5 View Scheme | |
Multi-step reaction with 3 steps 1: diethyl ether; toluene; methanol / 0.5 h / 0 °C / Inert atmosphere 2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 4 h / 20 °C 3: potassium hydroxide; water / 3 h / 100 °C View Scheme |
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With thionyl chloride for 2h; Heating / reflux; | 93% |
6-Chloro-3-pyridinecarboxylic acid
4-bromo-aniline
N-(4-bromophenyl)-6-chloronicotinamide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Reflux; | 93% |
6-Chloro-3-pyridinecarboxylic acid
Triethyl orthoacetate
6-chloro-3-pyridinecarboxylic acid ethyl ester
Conditions | Yield |
---|---|
In toluene | 92.3% |
6-Chloro-3-pyridinecarboxylic acid
tert–butyl (2–aminophenyl)carbamate
t-butyl (2-(6-chloronicotinamido)phenyl)carbamate
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 20℃; for 18h; | 92% |
With TEA; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate In acetonitrile at 20℃; |
Conditions | Yield |
---|---|
Stage #1: 6-Chloro-3-pyridinecarboxylic acid; cyclohexanol With sodium hydride In DMF (N,N-dimethyl-formamide) at 20℃; for 4h; Heating / reflux; Stage #2: With acetic acid In DMF (N,N-dimethyl-formamide); water pH=5; | 92% |
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 130℃; Inert atmosphere; | 76% |
6-Chloro-3-pyridinecarboxylic acid
6,6-difluoro-5-methyl-5-hexenol
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 15h; | 92% |
4-(2-AMINOETHYL)MORPHOLINE
6-Chloro-3-pyridinecarboxylic acid
6-chloro-N-(2-morpholinoethyl)nicotinamide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Reflux; | 92% |
methanol
6-Chloro-3-pyridinecarboxylic acid
6-Chloronicotinic acid methyl ester
Conditions | Yield |
---|---|
With sulfuric acid at 0 - 60℃; | 91% |
Stage #1: 6-Chloro-3-pyridinecarboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide at 20℃; for 16h; Stage #2: methanol In dichloromethane at 40℃; for 0.25h; | 91% |
With sulfuric acid for 8h; Reflux; Large scale; | 84.6% |
6-Chloro-3-pyridinecarboxylic acid
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 91% |
6-Chloro-3-pyridinecarboxylic acid
2-amino-benzenethiol
6-aminopyridine-3-carboxylic acid
Conditions | Yield |
---|---|
With acetic acid for 24h; Heating; | 90% |
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