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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiry2,4-Dichloropyrimidine-5-carboxylic acid Application:2,4-Dichloropyrimidine-5-carboxylic acid
2,4-dihydroxypyrimidine-5-carboxylic acid
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
With phosphorus pentachloride; trichlorophosphate Reflux; | 100% |
With N,N-diethylaniline; trichlorophosphate In N,N-dimethyl-formamide at 90℃; for 2.66667h; Under cold conditions; | 65% |
With N,N-diethylaniline; trichlorophosphate | |
With N,N-dimethyl-aniline; trichlorophosphate at 110℃; for 4h; Cooling with ice; |
2,4-dichloropyrimidine-5-carbonyl chloride
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
With water In diethyl ether at 35℃; for 1h; | 93% |
With water In tetrahydrofuran at 20℃; for 0.83h; |
2,4-dichloro-5-pyrimidinecarboxylic acid
6-nitropyridine-2-sulfonamide
Conditions | Yield |
---|---|
Stage #1: 2,4-dichloropyrimidine-5-carboxylic acid With thionyl chloride for 2h; Reflux; Stage #2: 6-nitropyridine-2-sulfonamide With triethylamine In dichloromethane at 20℃; for 0.5h; | 100% |
Stage #1: 2,4-dichloropyrimidine-5-carboxylic acid With thionyl chloride for 1h; Reflux; Stage #2: 6-nitropyridine-2-sulfonamide With trimethylamine In dichloromethane at 20℃; for 0.5h; | 100% |
2,4-dichloro-5-pyrimidinecarboxylic acid
2,4-dichloropyrimidine-5-carbonyl chloride
Conditions | Yield |
---|---|
With thionyl chloride at 80℃; for 4h; | 90% |
With phosphorus pentachloride; trichlorophosphate at 115℃; for 6h; | 64% |
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 1h; | |
With thionyl chloride Reflux; |
2,4-dichloro-5-pyrimidinecarboxylic acid
2,6-dimethyl-4-fluoroaniline
C13H10Cl2FN3O
Conditions | Yield |
---|---|
With Amberlyst A-21 resin In ethyl acetate at 50℃; | 90% |
2,4-dichloro-5-pyrimidinecarboxylic acid
aniline
2,4-dichloro-N-phenylpyrimidin-5-carboxamide
Conditions | Yield |
---|---|
With Amberlyst A-21 resin In ethyl acetate at 50℃; | 90% |
2,4-dichloro-5-pyrimidinecarboxylic acid
2,6-dimethylaniline
2,4-dichloro-N-(2,6-dimethylphenyl)pyrimidin-5-carboxamide
Conditions | Yield |
---|---|
With Amberlyst A-21 resin In ethyl acetate at 50℃; | 90% |
2,4-dichloro-5-pyrimidinecarboxylic acid
2,4,6-trimethylaniline
C14H13Cl2N3O
Conditions | Yield |
---|---|
With Amberlyst A-21 resin In ethyl acetate at 50℃; | 90% |
2,4-dichloro-5-pyrimidinecarboxylic acid
2,6-Dichloroaniline
2,4-dichloro-N-(2,6-dichlorophenyl)pyrimidine-5-carboxamide
Conditions | Yield |
---|---|
With Amberlyst A-21 resin In ethyl acetate at 50℃; | 90% |
2,4-dichloro-5-pyrimidinecarboxylic acid
N-Boc-1,3-diaminopropane
4-(3-tert-Butoxycarbonylaminopropylamino)-2-chloropyrimidine-5-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran; ethyl acetate at 2 - 20℃; for 0.5h; | 88.6% |
2,4-dichloro-5-pyrimidinecarboxylic acid
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
Stage #1: 2,4-dichloropyrimidine-5-carboxylic acid With lithium diisopropyl amide In tetrahydrofuran for 0.333333h; Inert atmosphere; Cooling with acetone-dry ice; Stage #2: N,N-dimethyl-formamide In tetrahydrofuran for 1h; | 70% |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Stage #1: 2,4-dichloropyrimidine-5-carboxylic acid With oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 16h; Stage #2: 4-aminotricyclo[3.3. 1.13,7]decan-1-ol With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide at 0℃; for 4h; | 66% |
2,4-dichloro-5-pyrimidinecarboxylic acid
1-Amino-2-methyl-propan-2-ol
2-Chloro-4-(2-hydroxy-2-methylpropylamino)pyrimidine-5-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 2 - 20℃; | 59% |
2,4-dichloro-5-pyrimidinecarboxylic acid
Cyclopentamine
2-chloro-4-(cyclopentylamino)pyrimidine-5-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 2 - 20℃; for 2h; | 42% |
spiro[2.5]octan-6-ylmethanol
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at 0℃; for 1.5h; |
2,4-dichloro-5-pyrimidinecarboxylic acid
ethylamine
2-chloro-4-(ethylamino)pyrimidine-5-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran; water at 20℃; for 1.75h; |
2,4-dichloro-5-pyrimidinecarboxylic acid
tert-Butyl [3-(2-chloro-5-fluorocarbonylpyrimidin-4-ylamino)propyl]-carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / ethyl acetate; tetrahydrofuran / 0.5 h / 2 - 20 °C 2: triethylamine; trifluoro-[1,3,5]triazine / dichloromethane / 2 h / 20 °C View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
2-Chloro-4-(2-hydroxy-2-methylpropylamino)pyrimidine-5-carboxylic acid fluoride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran / 2 - 20 °C 2: triethylamine; trifluoro-[1,3,5]triazine / dichloromethane / 20 °C View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / water; tetrahydrofuran / 1.75 h / 20 °C 2: triethylamine; trifluoro-[1,3,5]triazine / dichloromethane / 3 h View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
2-chloro-4-(cyclopentylamino)pyrimidine-6-carboxylic acid fluoride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran / 2 h / 2 - 20 °C 2: triethylamine; trifluoro-[1,3,5]triazine / dichloromethane / 4 h / 20 °C View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 16 h / 20 °C 1.2: 4 h / 0 °C 2.1: sodium carbonate / N,N-dimethyl acetamide / 4 h / 25 °C 3.1: tetrahydrofuran / 6 h / 150 °C / Microwave irradiation View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 16 h / 20 °C 1.2: 4 h / 0 °C 2.1: sodium hexamethyldisilazane / 2 h / 150 °C / Microwave irradiation 3.1: 10 h / 150 °C / Microwave irradiation View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 16 h / 20 °C 1.2: 4 h / 0 °C 2.1: sodium carbonate / N,N-dimethyl acetamide / 4 h / 25 °C View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 16 h / 20 °C 1.2: 4 h / 0 °C 2.1: sodium hexamethyldisilazane / 2 h / 150 °C / Microwave irradiation View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 16 h / 20 °C 1.2: 4 h / 0 °C 2.1: sodium carbonate / N,N-dimethyl acetamide / 4 h / 25 °C 3.1: tetrahydrofuran / 6 h / 150 °C / Microwave irradiation View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: thionyl chloride / 2 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride; water; iron / tetrahydrofuran; ethanol / 1 h / 60 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: thionyl chloride / 1 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride / water; ethanol; tetrahydrofuran / 1 h / 60 °C View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: thionyl chloride / 2 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride; water; iron / tetrahydrofuran; ethanol / 1 h / 60 °C 3.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 125 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: thionyl chloride / 1 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride / water; ethanol; tetrahydrofuran / 1 h / 60 °C 3.1: potassium carbonate / dimethyl sulfoxide / 20 h / 125 °C / Sealed tube View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: thionyl chloride / 2 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride; water; iron / tetrahydrofuran; ethanol / 1 h / 60 °C 3.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 125 °C 4.1: sodium carbonate / 1,4-dioxane / 1 h / 120 °C / Inert atmosphere; Microwave irradiation View Scheme | |
Multi-step reaction with 4 steps 1.1: thionyl chloride / 1 h / Reflux 1.2: 0.5 h / 20 °C 2.1: hydrogenchloride / water; ethanol; tetrahydrofuran / 1 h / 60 °C 3.1: potassium carbonate / dimethyl sulfoxide / 20 h / 125 °C / Sealed tube 4.1: sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 1 h / 120 °C / Microwave irradiation; Inert atmosphere View Scheme |
2,4-dichloro-5-pyrimidinecarboxylic acid
Cyclopropylamine
2-chloro-4-(cyclopropylamino)pyrimidine-5-carboxylic acid
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 70℃; for 0.166667h; Microwave irradiation; |
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