tetrahydrofuran
ethylenediamine
A
1-(2-aminoethyl)pyrrolidine
B
1,2-di(pyrrolidin-1-yl)ethane
Conditions | Yield |
---|---|
titanium(IV) oxide at 250 - 300℃; Yields of byproduct given; | A 87% B n/a |
titanium(IV) oxide at 250 - 300℃; Yield given; | A 87% B n/a |
2-(2-pyrrolidinylethyl)-1H-isoindole-1,3(2H)-dione
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 24h; Reflux; | 82% |
With hydrogenchloride | |
With hydrazine hydrate In ethanol at 20℃; |
N-cyanomethyl pyrrolidine
A
1-(2-aminoethyl)pyrrolidine
B
Bis<2-(pyrrolidin-1-yl)ethyl>amine
Conditions | Yield |
---|---|
With methanol; nickel at 50℃; under 88260.9 Torr; Hydrogenation; |
1,4-dibromo-butane
ethanol
ethylenediamine
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With ammonium hydroxide for 0.5h; |
N-(2-Pyrrolidin-1-yl-ethyl)-propionamide
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With hydrogenchloride for 16h; Heating; Yield given; |
Conditions | Yield |
---|---|
With ethanol |
N-cyanomethyl pyrrolidine
A
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With nickel at 85℃; Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: toluene 2: aqueous hydrochloric acid View Scheme |
1-(2-aminoethyl)pyrrolidine
Δ2-Cyclopentenylphenylacetyl chloride
N-<2-(1-Pyrrolidinyl)ethyl>-Δ2-cyclopentenylphenylacetamide
Conditions | Yield |
---|---|
In benzene for 0.25h; Heating; | 100% |
Conditions | Yield |
---|---|
In methanol at 25℃; for 3h; | 100% |
1-(2-aminoethyl)pyrrolidine
3-(4-oxo-1-piperidinyl)-benzonitrile
3-[4-[[2-(1-pyrrolidinyl)ethyl]amino]-1-piperidinyl]benzonitrile
Conditions | Yield |
---|---|
Stage #1: 1-(2-aminoethyl)pyrrolidine; 3-(4-oxo-1-piperidinyl)-benzonitrile With titanium(IV) isopropylate In dichloromethane at 20℃; Stage #2: With methanol; sodium cyanoborohydride In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
With 2-hydroxypyridin at 50℃; for 14h; | 100% |
1-(2-aminoethyl)pyrrolidine
2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester
4-methyl-2-[(2-pyrrolidin-1-yl-ethylcarbamoyl)-methyl]-1H-pyrrole-3-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; Cooling with ice; | 100% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; | 100% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; Cooling; |
1-(2-aminoethyl)pyrrolidine
di-tert-butyl dicarbonate
(2-pyrrolidin-1-ylethyl)carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; | 100% |
In tetrahydrofuran at 20℃; for 10h; | 78% |
With sodium hydrogencarbonate In tetrahydrofuran; water at 0 - 20℃; for 8h; |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
Stage #1: 1-(2-aminoethyl)pyrrolidine; 3,4'-difluoro-4-nitro-biphenyl In acetonitrile for 0.25h; Stage #2: With N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; | 100% |
1-(2-aminoethyl)pyrrolidine
2,3,4-tris((4-methoxybenzyl)oxy)benzoic acid
2,3,4-tris((4-methoxybenzyl)oxy)-N-(2-(pyrrolidin-1-yl)ethyl)benzamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 100% |
1-(2-aminoethyl)pyrrolidine
3,4-bis(benzyloxy)-2-methoxy-N-(2-(pyrrolidin-1-yl)ethyl)benzamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: benzenesulfonyl chloride With triethylamine In dichloromethane at 20℃; Stage #2: 1-(2-aminoethyl)pyrrolidine In dichloromethane | 100% |
1-(2-aminoethyl)pyrrolidine
Ethyl 9-chloro-5,6-difluoro-3-oxo-3H-pyrido[3,2,1-kl]phenoxazine-2-carboxylate
Conditions | Yield |
---|---|
With aluminum (III) chloride In tetrahydrofuran at 20℃; | 99% |
With aluminum (III) chloride In dichloromethane at 20℃; for 1h; |
1-(2-aminoethyl)pyrrolidine
2,3-bis((4-methoxybenzyl)oxy)benzoic acid
2,3-bis((4-methoxybenzyl)oxy)-N-(2-(pyrrolidin-1-yl)ethyl)benzamide
Conditions | Yield |
---|---|
Stage #1: 2,3-bis((4-methoxybenzyl)oxy)benzoic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h; Cooling with ice; Stage #2: 1-(2-aminoethyl)pyrrolidine In dichloromethane at 20℃; for 3h; Cooling with ice; | 99% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 99% |
1-(2-aminoethyl)pyrrolidine
2,4-dichloroquinazoline
2-chloro-N-<2-(1-pyrrolidinyl)ethyl>-4-quinazolinamine
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 12h; | 98% |
With N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 18h; | 65% |
In diethyl ether for 1.5h; | 56% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; 3 A molecular sieve In dichloromethane | 98% |
1-(2-aminoethyl)pyrrolidine
dimethyl 1-[3-(diethoxyphosphoryl)ethyl]-1H-1,2,3-triazole-4,5-dicarboxylate
diethyl [2-[4,5-bis[[2-(1-pyrrolidinyl)ethylamino]carbonyl]-1H-1,2,3-triazol-1-yl]ethyl]phosphonate
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 98% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 20℃; for 4.5h; | 98% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 20℃; for 4.5h; Inert atmosphere; | 98% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 4.5h; | 98% |
1-(2-aminoethyl)pyrrolidine
N-tert-butoxycarbonyl glutamic acid tert-butyl ester
Conditions | Yield |
---|---|
With HATU In tetrahydrofuran at 20℃; Cooling with ice; | 98% |
1-(2-aminoethyl)pyrrolidine
sulindac sulfide
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In acetonitrile at 20℃; Inert atmosphere; | 98% |
1-(2-aminoethyl)pyrrolidine
2,9‐bis(4-formylphenyl)‐1,10‐phenanthroline
Conditions | Yield |
---|---|
In ethanol for 5h; Reflux; | 98% |
Conditions | Yield |
---|---|
With ammonium acetate In ethanol at 80℃; for 9h; Catalytic behavior; Reagent/catalyst; Solvent; Green chemistry; | 98% |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With triethylamine In toluene at 80℃; for 6h; | 98% |
1-(2-aminoethyl)pyrrolidine
2-methyl-3H-naphtho[1,2-d]imidazole-5,6-dicarboxylic anhydride
Conditions | Yield |
---|---|
In ethanol; toluene Heating; | 97% |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
In ethanol at 80℃; | 96.7% |
1-(2-aminoethyl)pyrrolidine
C24H24O6
3,4-bis((4-methoxybenzyl)oxy)-2-methyl-N-(2-(pyrrolidin-1-yl)ethyl)benzamide
Conditions | Yield |
---|---|
Stage #1: C24H24O6 With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h; Cooling with ice; Stage #2: 1-(2-aminoethyl)pyrrolidine In dichloromethane at 20℃; Cooling with ice; | 96% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 96% |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
at 160 - 165℃; for 15h; Inert atmosphere; Sealed tube; | 96% |
Conditions | Yield |
---|---|
Stage #1: 2α,3β-diacetoxyoleane 12-ene-28-carboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 25℃; for 1h; Stage #2: 1-(2-aminoethyl)pyrrolidine In dichloromethane at 25℃; for 2h; | 96% |
Stage #1: 2α,3β-diacetoxyoleane 12-ene-28-carboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 25℃; for 1h; Stage #2: 1-(2-aminoethyl)pyrrolidine at 25℃; for 2h; | 96% |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; | 95.7% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; |
1-(2-aminoethyl)pyrrolidine
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 72h; | 95.3% |
1-(2-aminoethyl)pyrrolidine
3-acetylaminonaphthalene-1,8-dicarboxylic anhydride
N-[1,3-Dioxo-2-(2-pyrrolidin-1-yl-ethyl)-2,3-dihydro-1H-benzo[de]isoquinolin-5-yl]-acetamide
Conditions | Yield |
---|---|
In ethanol for 2h; Ambient temperature; | 95% |
1-chloro-4-nitro-9H-xanthen-9-one
1-(2-aminoethyl)pyrrolidine
4-nitro-1-(2-pyrrolidin-1-yl-ethylamino)-xanthen-9-one
Conditions | Yield |
---|---|
With pyridine Heating; | 95% |
With pyridine Heating; |
Molecule structure of 1-(2-Aminoethyl)pyrrolidine (CAS NO.7154-73-6):
IUPAC Name: 2-Pyrrolidin-1-ylethanamine
Molecular Weight: 114.18876 [g/mol]
Molecular Formula: C6H14N2
Index of Refraction: 1.488
Molar Refractivity: 34.87 cm3
Molar Volume: 121 cm3
Surface Tension: 36.1 dyne/cm
Density: 0.943 g/cm3
Flash Point: 47.8 °C
Enthalpy of Vaporization: 40.07 kJ/mol
Boiling Point: 164.1 °C at 760 mmHg
Vapour Pressure: 1.99 mmHg at 25 °C
Storage temp.: Flammables area
Sensitive: air sensitive
XLogP3: 0.1
H-Bond Donor: 1
H-Bond Acceptor: 2
Rotatable Bond Count: 2
Exact Mass: 114.115698
MonoIsotopic Mass: 114.115698
Topological Polar Surface Area: 29.3
Heavy Atom Count: 8
Complexity: 57.5
Canonical SMILES: C1CCN(C1)CCN
InChI: InChI=1S/C6H14N2/c7-3-6-8-4-1-2-5-8/h1-7H2
InChIKey: WRXNJTBODVGDRY-UHFFFAOYSA-N
EINECS: 230-509-5
Product Categories of 1-(2-Aminoethyl)pyrrolidine (CAS NO.7154-73-6): Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines; Heterocycles; Nitro/Nitriles
Hazard Codes: C
Risk Statements: 10-34
R10:Flammable.
R34:Causes burns.
Safety Statements: 16-26-27-36/37/39-45
S16:Keep away from sources of ignition.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S27:Take off immediately all contaminated clothing.
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.)
RIDADR: UN 2734 8/PG 2
WGK Germany: 3
F: 9-23
HazardClass: 3
PackingGroup: III
1-(2-Aminoethyl)pyrrolidine (CAS NO.7154-73-6) is also called 2-(1-Pyrrolidinyl)ethylamine ; 2-Pyrrolidinoethyl amine ; N-(2-Aminoethyl)pyrrolidine ; NSC 73740 ; Pyrrolidine, 1-(2-aminoethyl)- ; Pyrrolidinoethanamine ; Pyrrolidinoethylamine ; 1-Pyrrolidineethanamine ; N-(2-Aminoethyl)pyrrolidine . 1-(2-Aminoethyl)pyrrolidine (CAS NO.7154-73-6) is clear colorless to light brpwn liquid.
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