Product Name

  • Name

    1-(2-Aminoethyl)imidazolidin-2-one

  • EINECS 228-491-9
  • CAS No. 6281-42-1
  • Article Data20
  • CAS DataBase
  • Density 1.137 g/cm3
  • Solubility
  • Melting Point
  • Formula C5H11N3O
  • Boiling Point 363.1 °C at 760 mmHg
  • Molecular Weight 129.162
  • Flash Point 173.4 °C
  • Transport Information
  • Appearance
  • Safety 22-26-36/37/39-45
  • Risk Codes 34
  • Molecular Structure Molecular Structure of 6281-42-1 (1-(2-Aminoethyl)imidazolidin-2-one)
  • Hazard Symbols IrritantXi,CorrosiveC
  • Synonyms 1-(2-Aminoethyl)-2-imidazolidinone;1-(b-Aminoethyl)-2-imidazolidone;3-(2-Aminoethyl)-2-imidazolidinone;N-(2-Aminoethyl)imidazolidin-2-one;N-(2-Aminoethyl)imidazolidinone;N-(b-Aminoethyl)-N,N'-ethyleneurea;NSC 5776;[2-(2-Oxoimidazolidino)ethyl]amine;
  • PSA 58.36000
  • LogP -0.06270

Synthetic route

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

urea
57-13-6

urea

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With ammonia at 125 - 160℃; Concentration; Temperature; Inert atmosphere; Large scale;96%
at 210℃;
at 130 - 210℃; for 3h;
carbon dioxide
124-38-9

carbon dioxide

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With cerium(IV) oxide In ethanol at 160℃; for 8h;36%
With ethanolamine at 190℃; for 0.5h; Catalytic behavior; Reagent/catalyst;
1,3,6-triazabicyclo[3.3.0]oct-4-ene
6573-15-5

1,3,6-triazabicyclo[3.3.0]oct-4-ene

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With water
1-(2-chloroethyl)imidazolidin-2-one
2387-20-4

1-(2-chloroethyl)imidazolidin-2-one

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With ammonium hydroxide at 100℃;
1-(2-aminoethyl)-2-imidazolidinethione
40778-59-4

1-(2-aminoethyl)-2-imidazolidinethione

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With ammonium hydroxide; dihydrogen peroxide
Multi-step reaction with 2 steps
1: chloroacetic acid
2: H2O
View Scheme
1-(2-chloroethyl)imidazolidin-2-one
2387-20-4

1-(2-chloroethyl)imidazolidin-2-one

ammonium hydroxide

ammonium hydroxide

A

2-(2-amino-4,5-dihydro-imidazol-1-yl)-ethanol
98137-74-7

2-(2-amino-4,5-dihydro-imidazol-1-yl)-ethanol

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
at 100℃;
1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
With urea
bis-(2-phenylacetylamino-ethyl)-carbamic acid 4-nitro-phenyl ester
757967-03-6

bis-(2-phenylacetylamino-ethyl)-carbamic acid 4-nitro-phenyl ester

A

phenylacetic acid
103-82-2

phenylacetic acid

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C

4-nitro-phenol
100-02-7

4-nitro-phenol

D

(4-hydroxyphenyl)methanol
623-05-2

(4-hydroxyphenyl)methanol

E

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
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
111-40-0

1,5-diamino-3-azapentane

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

Conditions
ConditionsYield
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
3699-54-5

2-oxo-imidazolidine-1-ethanol

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

A

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

B

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

Conditions
ConditionsYield
at 270℃; for 5h; Autoclave; Inert atmosphere;A 30.5 %Chromat.
B 16.8 %Chromat.
imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

B

N,N'-diethylurea
623-76-7

N,N'-diethylurea

C

U2TETA
166532-70-3

U2TETA

D

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
24368-15-8

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)

E

U1TETA

U1TETA

F

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

G

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
With dimethylenecyclourethane at 260℃; for 1.5h; Inert atmosphere;
imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

B

U2TETA
166532-70-3

U2TETA

C

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
24368-15-8

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)

D

U1TETA

U1TETA

E

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

F

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
With dimethylenecyclourethane at 250℃; for 5.5h; Microwave irradiation; Inert atmosphere;
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C

U2TETA
166532-70-3

U2TETA

D

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
24368-15-8

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)

E

U1TETA

U1TETA

F

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

G

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
at 250℃; for 5.5h; Inert atmosphere;
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

D

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

E

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
at 260℃; for 3h;
imidazolidone
120-93-4

imidazolidone

ethanolamine
141-43-5

ethanolamine

ethylenediamine
107-15-3

ethylenediamine

A

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

B

U2TETA
166532-70-3

U2TETA

C

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
24368-15-8

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)

D

U1TETA

U1TETA

E

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

F

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
With dimethylenecyclourethane at 250℃; for 5h; Inert atmosphere;
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

11-mercaptounadecanoic acid
71310-21-9

11-mercaptounadecanoic acid

11-mercapto-N-[2-(2-oxoimidazolidin-1-yl)ethyl]undecaneamide

11-mercapto-N-[2-(2-oxoimidazolidin-1-yl)ethyl]undecaneamide

Conditions
ConditionsYield
at 160℃; for 6h; Inert atmosphere;100%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

1-(5-(methoxycarbonyl)-4-{[2-(trifluoromethyl)benzyl]oxy}thien-2-yl)-1H-benzimidazole-5-carboxylic acid
660870-46-2

1-(5-(methoxycarbonyl)-4-{[2-(trifluoromethyl)benzyl]oxy}thien-2-yl)-1H-benzimidazole-5-carboxylic acid

methyl 5-[5-({[2-(2-oxoimidazolidin-1-yl)ethyl]amino}carbonyl)-1H-benzimidazol-1-yl]-3-{[2-(trifluoromethyl)benzyl]oxy}thiophene-2-carboxylate

methyl 5-[5-({[2-(2-oxoimidazolidin-1-yl)ethyl]amino}carbonyl)-1H-benzimidazol-1-yl]-3-{[2-(trifluoromethyl)benzyl]oxy}thiophene-2-carboxylate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; HATU In DMF (N,N-dimethyl-formamide) for 2h;95%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

5-(4-chlorophenyl)-2-{[1-(4-chloropyridin-3-yl)-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

5-(4-chlorophenyl)-2-{[1-(4-chloropyridin-3-yl)-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

5-(4-chlorophenyl)-2-{[1-(4-{[2-(2-oxoimidazolidin-1-yl)ethyl]amino}pyridin-3-yl)-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

5-(4-chlorophenyl)-2-{[1-(4-{[2-(2-oxoimidazolidin-1-yl)ethyl]amino}pyridin-3-yl)-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

Conditions
ConditionsYield
In ethanol Reflux;94%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2-chloro-4-[7-(2-chloro-pyridin-4-yl)-benzo[b]thiophen-2-yl]-pyrimidine
1034658-89-3

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
1034657-98-1

1-(2-{4-[7-(2-chloro-pyridin-4-yl)-benzo[b]thiophen-2-yl]pyrimidin-2-ylamino}ethyl)imidazolidin-2-one

Conditions
ConditionsYield
In butan-1-ol at 120℃; for 5h;93%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2,4-dicyano-1-butene
1572-52-7

2,4-dicyano-1-butene

C11H17N5O

C11H17N5O

Conditions
ConditionsYield
In water at 75 - 80℃; Inert atmosphere;89%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

ethylene dibromide
106-93-4

ethylene dibromide

,4,7-triazacyclononan-1,4-one

,4,7-triazacyclononan-1,4-one

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20 - 100℃; for 60h; Reagent/catalyst; Solvent; Temperature;87.09%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

dichlorobenzenesulfonyl chloride
82417-45-6

dichlorobenzenesulfonyl chloride

2,3-dichloro-N-[2-(2-oxoimidazolidin-1-yl)ethyl]benzenesulphonamide
886236-60-8

2,3-dichloro-N-[2-(2-oxoimidazolidin-1-yl)ethyl]benzenesulphonamide

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃;87%
Divinyl sulfone
77-77-0

Divinyl sulfone

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

1-<2-N-(1,1-dioxidothiomorpholinoethyl)>-2-imidazolidinone
85694-70-8

1-<2-N-(1,1-dioxidothiomorpholinoethyl)>-2-imidazolidinone

Conditions
ConditionsYield
In ethanol for 3h; Ambient temperature;83%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

m-isopropenyl-α,α-dimethylbenzyl carbamic acid methyl ester
90826-32-7

m-isopropenyl-α,α-dimethylbenzyl carbamic acid methyl ester

Conditions
ConditionsYield
1,3-diacetoxy-1,1,3,3-tetrabutyldistannoxane at 140℃; under 30 Torr; for 3h;83%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

3,5-dimethyl-N-nitro-1H-pyrazole-1-carboxamidine
2946-89-6

3,5-dimethyl-N-nitro-1H-pyrazole-1-carboxamidine

N-nitro-N'-[2-(2-oxo-imidazolidin-3-yl)ethyl]guanidine

N-nitro-N'-[2-(2-oxo-imidazolidin-3-yl)ethyl]guanidine

Conditions
ConditionsYield
In methanol at 20℃;80%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐nitro‐1,2,5‐oxadiazol‐3‐yl)‐4,5‐dihydro‐1,2,4‐oxadiazol‐5‐one

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐nitro‐1,2,5‐oxadiazol‐3‐yl)‐4,5‐dihydro‐1,2,4‐oxadiazol‐5‐one

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐{[2‐(2‐oxoimidazolidin‐1‐yl)ethyl]amino}‐1,2,5‐oxadiazol‐3‐yl)‐1,2,4‐oxadiazol‐5‐one

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐{[2‐(2‐oxoimidazolidin‐1‐yl)ethyl]amino}‐1,2,5‐oxadiazol‐3‐yl)‐1,2,4‐oxadiazol‐5‐one

Conditions
ConditionsYield
In acetonitrile78%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

acrylic acid
79-10-7

acrylic acid

3,3'-{[2-(2-oxoimidazolidin-1-yl)ethyl]imino}dipropanoic acid

3,3'-{[2-(2-oxoimidazolidin-1-yl)ethyl]imino}dipropanoic acid

Conditions
ConditionsYield
In isopropyl alcohol at 60℃; for 2h; Inert atmosphere;75%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2-(methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine
893441-65-1

2-(methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine

1-(2-(4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

1-(2-(4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With triethylamine In toluene for 6h; Heating / reflux;72%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C18H12FNO2
1367126-25-7

C18H12FNO2

1-(2-(((6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)methyl)amino)ethyl)imidazolidin-2-one
1367124-97-7

1-(2-(((6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)methyl)amino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
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
6281-42-1

2-aminoethylimidazolidone

C20H18FNO4S
1367126-49-5

C20H18FNO4S

1-(2-((2-(6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)ethyl)amino)ethyl)imidazolidin-2-one
1367124-99-9

1-(2-((2-(6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)ethyl)amino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 40℃; for 14h;70%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

4-(5'-bromo-2'-thienyl)-2-chloropyrimidine
131022-68-9

4-(5'-bromo-2'-thienyl)-2-chloropyrimidine

1-(2-(4-(5-bromothiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

1-(2-(4-(5-bromothiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With triethylamine In isopropyl alcohol for 30h; Heating / reflux;68%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

3,4-dichlorophenylisocyanate
102-36-3

3,4-dichlorophenylisocyanate

C12H14Cl2N4O2

C12H14Cl2N4O2

Conditions
ConditionsYield
With triethylamine In toluene at 5℃; for 24h;68%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

4-chloro-3-formylcoumarin
50329-91-4

4-chloro-3-formylcoumarin

C15H15N3O4

C15H15N3O4

Conditions
ConditionsYield
With triethylamine In ethanol for 0.0833333h; Heating;67%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C19H10(2)H3F3N2O2

C19H10(2)H3F3N2O2

d-1-(2-(((6-(2-methyl-4-((5-(trifluoromethyl)pyridin-2-yl)oxy)-phenyl-3,5,6-d3)pyridin-2-yl)methyl)amino)ethyl)imidazolidin-2-one

d-1-(2-(((6-(2-methyl-4-((5-(trifluoromethyl)pyridin-2-yl)oxy)-phenyl-3,5,6-d3)pyridin-2-yl)methyl)amino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
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
6281-42-1

2-aminoethylimidazolidone

4-(benzo[b]thiophen-2-yl)-2-(methylsulfonyl)pyrimidine
893434-89-4

4-(benzo[b]thiophen-2-yl)-2-(methylsulfonyl)pyrimidine

1-(2-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

1-(2-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With triethylamine In 2-methoxy-ethanol at 100℃;64%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2-{[5-bromo-1-(2-chlorophenyl)-1H-1,2,4-triazol-3-yl]methyl}-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

2-{[5-bromo-1-(2-chlorophenyl)-1H-1,2,4-triazol-3-yl]methyl}-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

5-(4-chlorophenyl)-2-{[1-(2-chlorophenyl)-5-{[2-(2-oxoimidazolidin-1-yl)ethyl]amino}-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3 -one

5-(4-chlorophenyl)-2-{[1-(2-chlorophenyl)-5-{[2-(2-oxoimidazolidin-1-yl)ethyl]amino}-1H-1,2,4-triazol-3-yl]methyl}-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3 -one

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 150℃; for 5h; Microwave irradiation;64%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

{4-[2-(2-chloro-5-fluoro-pyrimidin-4-yl)-benzo[b]thiophen-7-yl]-6-fluoro-pyridin-3-ylmethyl}-dimethylamine
1034468-08-0

{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
1034466-20-0

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
ConditionsYield
With triethylamine In butan-1-ol at 120℃; for 15h;63%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2-[3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-1-yl]benzoyl chloride

2-[3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-1-yl]benzoyl chloride

2-[3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-1-yl]-N-[2-(2-oxoimidazolidin-1-yl)ethyl]benzamide

2-[3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-1-yl]-N-[2-(2-oxoimidazolidin-1-yl)ethyl]benzamide

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 1h;61%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

S-allyl isothiouronium hydrobromide
41848-21-9

S-allyl isothiouronium hydrobromide

hydroquinone
123-31-9

hydroquinone

2-(allylthio)-5-((2-(2-oxoimidazolidin-1-yl)ethyl)amino)-2,5-cyclohexadiene-1,4-dione

2-(allylthio)-5-((2-(2-oxoimidazolidin-1-yl)ethyl)amino)-2,5-cyclohexadiene-1,4-dione

Conditions
ConditionsYield
With sodium iodide; sodium chloride In water; acetonitrile at 20℃;58%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

N-acetyl-O-[bis(benzyloxy)phosphoryl]-L-tyrosine
151608-48-9

N-acetyl-O-[bis(benzyloxy)phosphoryl]-L-tyrosine

N-acetyl-O-[bis(benzyloxy)phosphoryl]-N'-[2-(2-oxoimidazolidin-1-yl)ethyl]-L-tyrosinamide
1268157-54-5

N-acetyl-O-[bis(benzyloxy)phosphoryl]-N'-[2-(2-oxoimidazolidin-1-yl)ethyl]-L-tyrosinamide

Conditions
ConditionsYield
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
6281-42-1

2-aminoethylimidazolidone

p-chlorphenylisocyanate
104-12-1

p-chlorphenylisocyanate

1-[2-(2-Oxo-3-imidazolidinyl)-ethyl]-3-(4-chlorophenyl)urea
63874-81-7

1-[2-(2-Oxo-3-imidazolidinyl)-ethyl]-3-(4-chlorophenyl)urea

Conditions
ConditionsYield
With triethylamine In toluene at 5℃; for 24h;53%
In tetrahydrofuran
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

4-(7-bromo-benzo[b]thiophen-2-yl)-2-chloro-5-fluoro-pyrimidine
1034468-28-4

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
1034468-55-7

1-{2-[4-(7-bromo-benzo[b]thiophen-2-yl)-5-fluoro-pyrimidin-2-ylamino]-ethyl}-imidazolidin-2-one

Conditions
ConditionsYield
In 1,4-dioxane at 90℃; for 3h;52%
2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

2-chloro-4-[7-(3-trimethylsilanylethynyl-pyridin-4-yl)-benzo[b]-thiophen-2-yl]-pyrimidine
1034468-45-5

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
1034468-65-9

1-(2-[4-[7-(3-trimethylsilylethynyl-pyridin-4-yl)-benzo[b]thiophen-2-yl]-pyrimidin-2-ylamino]-ethyl)-imidazolidin-2-one

Conditions
ConditionsYield
In butan-1-ol at 120℃; for 4 - 5h;49%

1-(2-Aminoethyl)-2-imidazolidone Chemical Properties

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

1-(2-Aminoethyl)-2-imidazolidone Production

Raw materials: Urea-->Diethylenetriamine

1-(2-Aminoethyl)-2-imidazolidone Safety Profile

Hazard Codes IrritantXi,CorrosiveC
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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