Conditions | Yield |
---|---|
With water for 0.5h; Heating; | 88% |
at 150℃; for 1h; | 64.1% |
for 0.5h; Reflux; | 63% |
Conditions | Yield |
---|---|
Stage #1: imidazolidone With potassium carbonate In toluene at 20℃; for 0.5h; Stage #2: 1-acetyl-1H-benzotriazole In toluene at 80℃; for 2h; | 87% |
imidazolidone
Benzyl isocyanide
acetyl chloride
A
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 9h; | A n/a B 77% |
Conditions | Yield |
---|---|
In tetrahydrofuran | 52% |
In tetrahydrofuran | 52% |
In tetrahydrofuran | 52% |
In tetrahydrofuran | 52% |
Conditions | Yield |
---|---|
With cerium(IV) oxide In ethanol at 160℃; for 8h; | 9% |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine In tetrahydrofuran at 80℃; for 9h; Inert atmosphere; Schlenk technique; | 94.4% |
1-acetylimidazolidin-2-one
bis(trichloromethyl) carbonate
1-chlorocarbonyl-2-oxo-3-methylcarbonyl-imidazolidine
Conditions | Yield |
---|---|
In benzene at 55 - 60℃; for 3h; chloroformylation; | 93.8% |
1-acetylimidazolidin-2-one
4-amino-5-chloro-2,1,3-benzothiadiazole
Conditions | Yield |
---|---|
With trichlorophosphate In acetone at 50 - 55℃; for 20h; Temperature; Solvent; | 93.6% |
With thionyl chloride In toluene at 65℃; Reagent/catalyst; Solvent; | 67% |
1-acetylimidazolidin-2-one
trichloromethyl chloroformate
1-chlorocarbonyl-2-oxo-3-methylcarbonyl-imidazolidine
Conditions | Yield |
---|---|
With pyridine In benzene at 50 - 55℃; for 2h; Addition; | 92% |
1-acetylimidazolidin-2-one
4-amino-5-chloro-2,1,3-benzothiadiazole
tizanidine hydrochloride
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 4-amino-5-chloro-2,1,3-benzothiadiazole With trichlorophosphate at 60 - 65℃; for 36h; Stage #2: With methanol for 4h; Reflux; Stage #3: With hydrogenchloride In ethanol at 20℃; for 1h; | 85% |
1-acetylimidazolidin-2-one
5-bromo-2-methyl-1H-indole
5-Bromo-3-(4,5-dihydroimidazol-2-yl)-2-methyl-1H-indole
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 5-bromo-2-methyl-1H-indole With trichlorophosphate at 50℃; Stage #2: With ethanol Heating; | 80% |
Stage #1: 1-acetylimidazolidin-2-one; 5-bromo-2-methyl-1H-indole With trichlorophosphate at 50℃; Stage #2: With ethanol Heating / reflux; |
Conditions | Yield |
---|---|
80% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
With phosphorus pentachloride In chloroform at 20℃; for 24h; | 79% |
Conditions | Yield |
---|---|
With trichlorophosphate for 3h; Condensation; Heating; | 74% |
1-acetylimidazolidin-2-one
4-aminoindan
N-(1-Acetyl-2-imidazolin-2-yl)-N-(4-indanyl)amin
Conditions | Yield |
---|---|
With trichlorophosphate at 50℃; for 40h; | 73.1% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
73% | |
15.8% |
1-acetylimidazolidin-2-one
4-amino-5-chloro-2,1,3-benzothiadiazole
tizanidine
Conditions | Yield |
---|---|
With trichlorophosphate In methanol; sodium hydroxide; water | 73% |
1-acetylimidazolidin-2-one
2-(4-methylphenyl)-5-trifluoromethoxy-1H-indole
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 2-(4-methylphenyl)-5-trifluoromethoxy-1H-indole With trichlorophosphate at 60℃; for 20h; Stage #2: In ethanol at 60℃; for 5h; | 70% |
1-acetylimidazolidin-2-one
4-amino-5-chloro-2,1,3-benzothiadiazole
tizanidine
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 4-amino-5-chloro-2,1,3-benzothiadiazole With trichlorophosphate at 60 - 65℃; for 36h; Stage #2: With methanol; sodium hydroxide for 4h; Reflux; | 70% |
1-acetylimidazolidin-2-one
2,6-diethylaniline
1-acetyl-N-(2,6-diethylphenyl)-4,5-dihydro-1H-imidazol-2(3H)-imine
Conditions | Yield |
---|---|
With trichlorophosphate for 3h; Heating; | 69.9% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
68% |
1-acetylimidazolidin-2-one
2-(4-methylphenyl)-5-chloro-1H-indole
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 2-(4-methylphenyl)-5-chloro-1H-indole With trichlorophosphate at 50℃; Stage #2: With ethanol Heating; | 67% |
1-acetylimidazolidin-2-one
2-ethyl-5-chloro-1H-indole
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 2-ethyl-5-chloro-1H-indole With trichlorophosphate at 50℃; Stage #2: With ethanol Heating; | 67% |
7.1% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; sodium hydroxide In toluene at 20℃; for 5h; | 67% |
Conditions | Yield |
---|---|
66% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
66% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
With trichlorophosphate Condensation; | 65% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
65% |
1-acetylimidazolidin-2-one
Conditions | Yield |
---|---|
64.8% | |
45% |
Conditions | Yield |
---|---|
Stage #1: 1-acetylimidazolidin-2-one; 5-methoxy-2-methyl-1H-indole With trichlorophosphate at 50℃; Stage #2: With ethanol Heating; | 64% |
14.6% |
1-acetylimidazolidin-2-one
diisopropyl hydrogenphosphonate
diisopropyl(3-acetyl-2-oxoimidazolidin-1-yl)phosphonate
Conditions | Yield |
---|---|
With 6,6'-dimethyl-2,2'-bipyridine; copper diacetate In toluene at 80℃; under 760.051 Torr; for 1.5h; Reagent/catalyst; Molecular sieve; | 64% |
Conditions | Yield |
---|---|
63.9% |
Product Name: 1-Acetyl-2-imidazolidinone (CAS NO.5391-39-9)
Molecular Formula: C5H8N2O2
Molecular Weight: 128.13g/mol
Mol File: 5391-39-9.mol
EINECS: 226-388-3
Melting Point: 173-175°C
Density: 1.237 g/cm3
Index of Refraction: 1.492 Molar Refractivity: 30.08 cm3
Molar Volume: 103.5 cm3
Surface Tension: 43.2 dyne/cm
XLogP3-AA: -0.9
H-Bond Donor: 1
H-Bond Acceptor: 2
Structure Descriptors of 1-Acetyl-2-imidazolidinone (CAS NO.5391-39-9):
IUPAC Name: 1-acetylimidazolidin-2-one
Canonical SMILES: CC(=O)N1CCNC1=O
InChI: InChI=1S/C5H8N2O2/c1-4(8)7-3-2-6-5(7)9/h2-3H2,1H3,(H,6,9)
InChIKey: JJWACYUTERPMBM-UHFFFAOYSA-N
Product Categories: Imidazol&Benzimidazole; (intermediate of moxonidine hcl)
1-Acetyl-2-imidazolidinone , its CAS NO. is 5391-39-9, the synonym is 1-Acetyl-2-imidazolidinone .
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