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Cas:5093-64-1
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Cas:5093-64-1
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inquiryProduct Name: 2-Acetamido-5-nitropyridine Synonyms: 2-ACETAMIDO-5-NITROPYRIDINE;[N-5-NITRO-2-PYRIDYL] ACETAMIDE;2-Acetamido-5-nitropyridine ,98%;N-(5-nitropyridin-2-yl)aceta CAS: 5093-64-1 MF: C7H7N3O3 MW: 181.15
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Min.Order:1 Kilogram
FOB Price: $8900.0
Type:Lab/Research institutions
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Min.Order:100 Gram
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Min.Order:1 Gram
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Min.Order:0 Metric Ton
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Cas:5093-64-1
Min.Order:1 Gram
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2-Acetamido-5-nitropyridine cas 5093-64-1Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquiry5-nitro-pyridin-2-ylamine
A
N-(5-aminopyridin-2-yl)acetamide
B
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
With sulfuric acid In acetic anhydride | A n/a B 98% |
Conditions | Yield |
---|---|
With pyridine; dmap at 0 - 20℃; | 86% |
With pyridine; dmap at 0 - 25℃; for 5h; | 86% |
at 130℃; for 1.5h; | 81% |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 0 - 20℃; for 2h; | 80.1% |
With triethylamine In dichloromethane at 20℃; for 6h; | 77% |
With dmap; triethylamine In tetrahydrofuran; ethyl acetate | |
With dmap; triethylamine In tetrahydrofuran for 24h; Heating / reflux; |
5-nitro-pyridin-2-ylamine
N,N-dimethyl acetamide
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl acetamide With 1,1'-carbonyldiimidazole at 120 - 125℃; for 0.5h; Inert atmosphere; Stage #2: 5-nitro-pyridin-2-ylamine at 60 - 65℃; for 5.5h; Inert atmosphere; | 70% |
dmap
5-nitro-pyridin-2-ylamine
acetyl chloride
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In dichloromethane | 49% |
With potassium carbonate; triethylamine In dichloromethane | 49% |
Conditions | Yield |
---|---|
Stage #1: acetamide With sodium hydride In dimethyl sulfoxide for 2h; Stage #2: 3-nitropyridine With potassium hexacyanoferrate(III) In dimethyl sulfoxide at 20℃; for 2h; | 34% |
Conditions | Yield |
---|---|
With dmap; N2; triethylamine In CH2C12 |
2-acetamido-5-nitropyridine
N-(5-aminopyridin-2-yl)acetamide
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol for 3.5h; | 98% |
With water; ammonium chloride; zinc In ethanol at 20℃; for 5h; | 84% |
With hydrogen; palladium on activated charcoal In methanol |
Conditions | Yield |
---|---|
In ethanol; chloroform | 20% |
In ethanol; chloroform | 20% |
Conditions | Yield |
---|---|
With 18-crown-6 ether In acetonitrile for 32h; Heating; |
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 18-crown-6 / acetonitrile / 32 h / Heating 2: aq. KHSO4; 18-crown-6; sodium chlorodifluoroacetate / acetonitrile / 1 h / Heating View Scheme |
2-acetamido-5-nitropyridine
toluene-4-sulfonic acid
C7H7N3O3*C7H8O3S
Conditions | Yield |
---|---|
In toluene for 2h; Reflux; |
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: zinc; ammonium chloride; water / ethanol / 5 h / 20 °C 2.1: thionyl chloride; triethylamine / dichloromethane / 4 h / 20 °C 2.2: 20 °C View Scheme |
2-acetamido-5-nitropyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C 3.1: triethylamine / ethanol / 3 h / pH 9.5 / Reflux View Scheme |
2-acetamido-5-nitropyridine
N-{4-[5-(acetylamino)-1H-pyrrolo[3,2-b]pyridin-2-yl]phenyl}-1-(phenylacetyl)-L-prolinamide
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C 3.1: triethylamine / ethanol / 3 h / pH 9.5 / Reflux 4.1: polyphosphoric acid / 1.25 h / 90 °C / Inert atmosphere 5.1: hydrogenchloride; water / 2 h / Reflux 6.1: HATU; N-ethyl-N,N-diisopropylamine / acetonitrile / 25 °C 7.1: triethylamine / acetonitrile / 0.6 h / 0 - 25 °C View Scheme |
2-acetamido-5-nitropyridine
C7H10N4O
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C View Scheme |
2-acetamido-5-nitropyridine
C17H16N4O2
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C 3.1: triethylamine / ethanol / 3 h / pH 9.5 / Reflux 4.1: polyphosphoric acid / 1.25 h / 90 °C / Inert atmosphere View Scheme |
2-acetamido-5-nitropyridine
C13H12N4
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C 3.1: triethylamine / ethanol / 3 h / pH 9.5 / Reflux 4.1: polyphosphoric acid / 1.25 h / 90 °C / Inert atmosphere 5.1: hydrogenchloride; water / 2 h / Reflux View Scheme |
2-acetamido-5-nitropyridine
C26H25N5O2
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 6 h / 2585.81 Torr 2.1: sodium nitrite; hydrogenchloride / water / 0.75 h / 0 °C 2.2: 16 h / 0 - 20 °C 3.1: triethylamine / ethanol / 3 h / pH 9.5 / Reflux 4.1: polyphosphoric acid / 1.25 h / 90 °C / Inert atmosphere 5.1: hydrogenchloride; water / 2 h / Reflux 6.1: HATU; N-ethyl-N,N-diisopropylamine / acetonitrile / 25 °C View Scheme |
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