Conditions | Yield |
---|---|
With ammonia at 125 - 160℃; Concentration; Temperature; Inert atmosphere; Large scale; | 96% |
at 210℃; | |
at 130 - 210℃; for 3h; |
Conditions | Yield |
---|---|
With cerium(IV) oxide In ethanol at 160℃; for 8h; | 36% |
With ethanolamine at 190℃; for 0.5h; Catalytic behavior; Reagent/catalyst; |
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With ammonium hydroxide at 100℃; |
1-(2-aminoethyl)-2-imidazolidinethione
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
With ammonium hydroxide; dihydrogen peroxide | |
Multi-step reaction with 2 steps 1: chloroacetic acid 2: H2O View Scheme |
1-(2-chloroethyl)imidazolidin-2-one
A
2-(2-amino-4,5-dihydro-imidazol-1-yl)-ethanol
B
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
at 100℃; |
Conditions | Yield |
---|---|
With urea |
bis-(2-phenylacetylamino-ethyl)-carbamic acid 4-nitro-phenyl ester
A
phenylacetic acid
B
2-aminoethylimidazolidone
C
4-nitro-phenol
D
(4-hydroxyphenyl)methanol
E
carbon dioxide
Conditions | Yield |
---|---|
With water; penicillin-G-amidase In Chremephor EL; dimethyl sulfoxide at 37℃; pH=7.4; Kinetics; Enzymatic reaction; Aqueous phosphate buffer; |
1,5-diamino-3-azapentane
carbonic acid dimethyl ester
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
With sodium methylate In methanol at 23 - 120℃; for 4h; Inert atmosphere; | |
With sodium methylate In methanol at 23 - 120℃; for 4h; Concentration; Solvent; Inert atmosphere; |
2-oxo-imidazolidine-1-ethanol
1,5-diamino-3-azapentane
A
2-aminoethylimidazolidone
B
2-(2-Aminoethylamino)ethanol
Conditions | Yield |
---|---|
at 270℃; for 5h; Autoclave; Inert atmosphere; | A 30.5 %Chromat. B 16.8 %Chromat. |
imidazolidone
ethylenediamine
A
2-aminoethylimidazolidone
B
N,N'-diethylurea
C
U2TETA
D
1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
F
1,5-diamino-3-azapentane
G
triethylentetramine
Conditions | Yield |
---|---|
With dimethylenecyclourethane at 260℃; for 1.5h; Inert atmosphere; |
imidazolidone
ethylenediamine
A
2-aminoethylimidazolidone
B
U2TETA
C
1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
E
1,5-diamino-3-azapentane
F
triethylentetramine
Conditions | Yield |
---|---|
With dimethylenecyclourethane at 250℃; for 5.5h; Microwave irradiation; Inert atmosphere; |
dimethylenecyclourethane
imidazolidone
ethylenediamine
A
2-oxo-imidazolidine-1-ethanol
B
2-aminoethylimidazolidone
C
U2TETA
D
1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
F
1,5-diamino-3-azapentane
G
triethylentetramine
Conditions | Yield |
---|---|
at 250℃; for 5.5h; Inert atmosphere; |
dimethylenecyclourethane
imidazolidone
ethylenediamine
A
2-oxo-imidazolidine-1-ethanol
B
2-aminoethylimidazolidone
C
2-(2-Aminoethylamino)ethanol
D
1,5-diamino-3-azapentane
E
triethylentetramine
Conditions | Yield |
---|---|
at 260℃; for 3h; |
imidazolidone
ethanolamine
ethylenediamine
A
2-aminoethylimidazolidone
B
U2TETA
C
1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
E
1,5-diamino-3-azapentane
F
triethylentetramine
Conditions | Yield |
---|---|
With dimethylenecyclourethane at 250℃; for 5h; Inert atmosphere; |
2-aminoethylimidazolidone
11-mercaptounadecanoic acid
Conditions | Yield |
---|---|
at 160℃; for 6h; Inert atmosphere; | 100% |
2-aminoethylimidazolidone
1-(5-(methoxycarbonyl)-4-{[2-(trifluoromethyl)benzyl]oxy}thien-2-yl)-1H-benzimidazole-5-carboxylic acid
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In DMF (N,N-dimethyl-formamide) for 2h; | 95% |
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
In ethanol Reflux; | 94% |
2-aminoethylimidazolidone
2-chloro-4-[7-(2-chloro-pyridin-4-yl)-benzo[b]thiophen-2-yl]-pyrimidine
1-(2-{4-[7-(2-chloro-pyridin-4-yl)-benzo[b]thiophen-2-yl]pyrimidin-2-ylamino}ethyl)imidazolidin-2-one
Conditions | Yield |
---|---|
In butan-1-ol at 120℃; for 5h; | 93% |
Conditions | Yield |
---|---|
In water at 75 - 80℃; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20 - 100℃; for 60h; Reagent/catalyst; Solvent; Temperature; | 87.09% |
2-aminoethylimidazolidone
dichlorobenzenesulfonyl chloride
2,3-dichloro-N-[2-(2-oxoimidazolidin-1-yl)ethyl]benzenesulphonamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; | 87% |
Divinyl sulfone
2-aminoethylimidazolidone
1-<2-N-(1,1-dioxidothiomorpholinoethyl)>-2-imidazolidinone
Conditions | Yield |
---|---|
In ethanol for 3h; Ambient temperature; | 83% |
2-aminoethylimidazolidone
m-isopropenyl-α,α-dimethylbenzyl carbamic acid methyl ester
m-TMU
Conditions | Yield |
---|---|
1,3-diacetoxy-1,1,3,3-tetrabutyldistannoxane at 140℃; under 30 Torr; for 3h; | 83% |
Conditions | Yield |
---|---|
In methanol at 20℃; | 80% |
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
In acetonitrile | 78% |
Conditions | Yield |
---|---|
In isopropyl alcohol at 60℃; for 2h; Inert atmosphere; | 75% |
2-aminoethylimidazolidone
2-(methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine
Conditions | Yield |
---|---|
With triethylamine In toluene for 6h; Heating / reflux; | 72% |
2-aminoethylimidazolidone
C18H12FNO2
1-(2-(((6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)methyl)amino)ethyl)imidazolidin-2-one
Conditions | Yield |
---|---|
Stage #1: 2-aminoethylimidazolidone; C18H12FNO2 In tetrahydrofuran at 20℃; for 14h; Stage #2: With sodium tetrahydroborate In tetrahydrofuran at 20℃; for 0.333333h; | 72% |
2-aminoethylimidazolidone
C20H18FNO4S
1-(2-((2-(6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)ethyl)amino)ethyl)imidazolidin-2-one
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 40℃; for 14h; | 70% |
2-aminoethylimidazolidone
4-(5'-bromo-2'-thienyl)-2-chloropyrimidine
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol for 30h; Heating / reflux; | 68% |
Conditions | Yield |
---|---|
With triethylamine In toluene at 5℃; for 24h; | 68% |
Conditions | Yield |
---|---|
With triethylamine In ethanol for 0.0833333h; Heating; | 67% |
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
Stage #1: 2-aminoethylimidazolidone; C19H10(2)H3F3N2O2 In methanol at 20℃; for 1h; Stage #2: With 5%-palladium/activated carbon; hydrogen In methanol at 20℃; under 760.051 Torr; for 3h; | 65% |
2-aminoethylimidazolidone
4-(benzo[b]thiophen-2-yl)-2-(methylsulfonyl)pyrimidine
Conditions | Yield |
---|---|
With triethylamine In 2-methoxy-ethanol at 100℃; | 64% |
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In acetonitrile at 150℃; for 5h; Microwave irradiation; | 64% |
2-aminoethylimidazolidone
{4-[2-(2-chloro-5-fluoro-pyrimidin-4-yl)-benzo[b]thiophen-7-yl]-6-fluoro-pyridin-3-ylmethyl}-dimethylamine
1-(2-{4-[7-(5-((dimethylamino)methyl)-2-fluoro-pyridin-4-yl)benzo[b]thiophen-2-yl]-5-fluoropyrimidin-2-ylamino}ethyl)imidazolidin-2-one
Conditions | Yield |
---|---|
With triethylamine In butan-1-ol at 120℃; for 15h; | 63% |
2-aminoethylimidazolidone
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; | 61% |
2-aminoethylimidazolidone
S-allyl isothiouronium hydrobromide
hydroquinone
Conditions | Yield |
---|---|
With sodium iodide; sodium chloride In water; acetonitrile at 20℃; | 58% |
2-aminoethylimidazolidone
N-acetyl-O-[bis(benzyloxy)phosphoryl]-L-tyrosine
N-acetyl-O-[bis(benzyloxy)phosphoryl]-N'-[2-(2-oxoimidazolidin-1-yl)ethyl]-L-tyrosinamide
Conditions | Yield |
---|---|
Stage #1: N-acetyl-O-[bis(benzyloxy)phosphoryl]-L-tyrosine With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: 2-aminoethylimidazolidone In dichloromethane at 0 - 20℃; for 2.16667h; Inert atmosphere; | 56% |
2-aminoethylimidazolidone
p-chlorphenylisocyanate
1-[2-(2-Oxo-3-imidazolidinyl)-ethyl]-3-(4-chlorophenyl)urea
Conditions | Yield |
---|---|
With triethylamine In toluene at 5℃; for 24h; | 53% |
In tetrahydrofuran |
2-aminoethylimidazolidone
4-(7-bromo-benzo[b]thiophen-2-yl)-2-chloro-5-fluoro-pyrimidine
1-{2-[4-(7-bromo-benzo[b]thiophen-2-yl)-5-fluoro-pyrimidin-2-ylamino]-ethyl}-imidazolidin-2-one
Conditions | Yield |
---|---|
In 1,4-dioxane at 90℃; for 3h; | 52% |
2-aminoethylimidazolidone
2-chloro-4-[7-(3-trimethylsilanylethynyl-pyridin-4-yl)-benzo[b]-thiophen-2-yl]-pyrimidine
1-(2-[4-[7-(3-trimethylsilylethynyl-pyridin-4-yl)-benzo[b]thiophen-2-yl]-pyrimidin-2-ylamino]-ethyl)-imidazolidin-2-one
Conditions | Yield |
---|---|
In butan-1-ol at 120℃; for 4 - 5h; | 49% |
IUPAC Name: 1-(2-Aminoethyl)imidazolidin-2-one
Synonyms: 1-(2-Aminoethyl)imidazolidin-2-one ; 2-Imidazolidinone, 1-(2-aminoethyl)- ; 1-(.beta.-Aminoethyl)-2-imidazolidone
Product Categories: Imidazoles & Benzimidazoles;Imidazoles & Benzimidazoles
Molecular Structure of 1-(2-Aminoethyl)-2-imidazolidone (CAS NO.6281-42-1):
Molecular Formula of 1-(2-Aminoethyl)-2-imidazolidone (CAS NO.6281-42-1): C5H11N3O
Molecular Weight of 1-(2-Aminoethyl)-2-imidazolidone (CAS NO.6281-42-1): 129.16
CAS NO: 6281-42-1
EINECS : 228-491-9
Index of Refraction: 1.506
Surface Tension: 42.6 dyne/cm
Density: 1.137 g/cm3
Flash Point: 173.4 °C
Enthalpy of Vaporization: 60.91 kJ/mol
Boiling Point: 363.1 °C at 760 mmHg
Vapour Pressure: 1.85E-05 mmHg at 25°C
Raw materials: Urea-->Diethylenetriamine
Hazard Codes Xi,C
Risk Statements 34
R34:Causes burns.
Safety Statements 22-26-36/37/39-45
S22:Do not breathe dust.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
Hazard Note Irritant
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