2-(3-diethylaminopropyl)-1H-isoindole-1,3(2H)-dione
diethylaminopropylamine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 24h; Reflux; | 73% |
With hydrazine hydrate In ethanol for 3h; Reflux; | 14% |
With hydrazine |
Conditions | Yield |
---|---|
With ethanol; sodium for 3h; Reflux; | 56% |
With sodium-potassium alloy; butan-1-ol | |
With ethanol; sodium |
Conditions | Yield |
---|---|
With xylene Hydrolyse des entstandenen N-<3-Diaethylamino-propyl>-phthalimids mit konz.HCl bei Siedetemperatur.; | |
With xylene Hydrolyse des entstandenen N-<3-Diaethylamino-propyl>-phthalimids mit konz.HCl bei Siedetemperatur.; |
2-(3-bromopropyl)isoindole-1,3-dione
diethylamine
diethylaminopropylamine
Conditions | Yield |
---|---|
Hydrolyse des entstandenen N-<3-Diaethylamino-propyl>-phthalimids mit konz.HCl bei Siedetemperatur.; | |
(i) KOH, MeOH, (ii) aq. KOH, (heating); Multistep reaction; | |
Hydrolyse des entstandenen N-<3-Diaethylamino-propyl>-phthalimids mit konz.HCl bei Siedetemperatur.; |
3-diethylaminopropionitrile
A
bis-(3-diethylamino-propyl)-amine
B
diethylaminopropylamine
Conditions | Yield |
---|---|
With sodium-potassium alloy; butan-1-ol | |
With nickel at 100℃; under 62518.2 Torr; Hydrogenation; |
tetra-N-ethyl-ξ-propenediyldiamine
diethylaminopropylamine
Conditions | Yield |
---|---|
With ammonia; nickel at 100℃; under 91938.4 Torr; Hydrogenation; | |
With ammonia; nickel at 100℃; under 91938.4 Torr; Hydrogenation; |
diethylamine
propan-1-ol-3-amine
A
1-amino-2-propene
B
diethylaminopropylamine
Conditions | Yield |
---|---|
With thorium dioxide at 270 - 290℃; |
azetidine
diethylamine
A
1-<(3-aminopropyl)aminopropyl>diethylamine
B
diethylaminopropylamine
Conditions | Yield |
---|---|
With perchloric acid at 25℃; Rate constant; Thermodynamic data; E(a), ΔS(excit.); |
diethylaminopropylamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
3-diethylaminopropionitrile
A
bis-(3-diethylamino-propyl)-amine
B
diethylaminopropylamine
Conditions | Yield |
---|---|
Hydrogenation; |
3-diethylaminopropionitrile
butan-1-ol
A
bis-(3-diethylamino-propyl)-amine
B
diethylaminopropylamine
3-diethylaminopropionitrile
ethanol
A
bis-(3-diethylamino-propyl)-amine
B
diethylaminopropylamine
3-diethylaminopropionitrile
butan-1-ol
A
bis-(3-diethylamino-propyl)-amine
B
diethylaminopropylamine
6-chloro-5-ethylamino-3-methoxy-pyrazine-2-carboxylic acid 3-diethylamino-propylamide
A
diethylaminopropylamine
B
6-chloro-5-ethylamino-3-methoxy-pyrazine-2-carboxylic acid
diethylamine
acrolein
A
diethylaminopropylamine
B
3-Methylpiperidine
Conditions | Yield |
---|---|
Stage #1: diethylamine; acrolein In tetrahydrofuran at 4℃; Stage #2: With ammonia; hydrogen; Raney cobalt In tetrahydrofuran at 80℃; under 45004.5 Torr; for 6h; Product distribution / selectivity; autoclave; | A 52 %Chromat. B 8 %Chromat. |
Conditions | Yield |
---|---|
Stage #1: diethylamine; acrolein In tetrahydrofuran at 4℃; Stage #2: With ammonia; hydrogen; Raney cobalt In tetrahydrofuran at 80℃; under 45004.5 Torr; for 6h; Product distribution / selectivity; autoclave; | 87 %Chromat. |
N-(3-(diethylamino)-propyl)benzamide
A
diethylaminopropylamine
B
benzyl alcohol
Conditions | Yield |
---|---|
With Ag/γ-Al2O3 (5 mol%); potassium tert-butylate; hydrogen In 1,4-dioxane at 170℃; under 45004.5 Torr; for 120h; Green chemistry; chemoselective reaction; | A 83 %Spectr. B 84 %Spectr. |
N-{3-[4-(6-chloropyridin-3-yl)-pyrimidin-2-ylamino]-4-methylphenyl}-3-trifluoromethylbenzamide
diethylaminopropylamine
Conditions | Yield |
---|---|
at 110℃; | 100% |
Conditions | Yield |
---|---|
Stage #1: C36H28Cl2N12O8S2(2-)*2Na(1+); diethylaminopropylamine In water at 70 - 97℃; for 4h; Stage #2: With hydrogenchloride In water pH=4.5; | 100% |
Conditions | Yield |
---|---|
In methanol; sodium hydroxide; dichloromethane; chloroform | 100% |
3-bromobenzoyl chloride
diethylaminopropylamine
3-bromo-N-(3-diethylamino-propyl)benzamide
Conditions | Yield |
---|---|
With sodium hydroxide In dichloromethane; water at 0 - 20℃; for 18h; Cooling with ice; Inert atmosphere; | 100% |
With sodium hydroxide In dichloromethane; water at 0 - 20℃; for 18h; Product distribution / selectivity; Inert atmosphere; | 99% |
2-Chloro-3-diisopropylaminocarbonylpyridine
diethylaminopropylamine
Conditions | Yield |
---|---|
at 150℃; for 1h; | 99% |
diethylaminopropylamine
4-(4-Methoxy-phenyl)-3-oxiranylmethoxymethyl-butan-1-ol
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 99% |
acetic anhydride
diethylaminopropylamine
3-diethylaminopropyl-1-acetamide
Conditions | Yield |
---|---|
With pyridine for 18h; Ambient temperature; | 99% |
diethylaminopropylamine
4-Benzo[1,3]dioxol-5-yl-3-oxiranylmethoxymethyl-butan-1-ol
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 98% |
Conditions | Yield |
---|---|
Stage #1: C38H32Cl2N12O10S2(2-)*2Na(1+); diethylaminopropylamine In water at 70 - 98℃; for 4h; Stage #2: With hydrogenchloride In water pH=2.0; | 98% |
di-tert-butyl dicarbonate
diethylaminopropylamine
tert-butyl 3-(diethylamino)propylcarbamate
Conditions | Yield |
---|---|
at 20℃; | 98% |
(+)-usnic acid
diethylaminopropylamine
Conditions | Yield |
---|---|
In ethanol for 3h; Reflux; | 98% |
sulindac sulfide
diethylaminopropylamine
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In acetonitrile at 20℃; Inert atmosphere; | 98% |
1-chloro-7-methoxy-4-nitro-10H-acridin-9-one
diethylaminopropylamine
1-(3-Diethylamino-propylamino)-7-methoxy-4-nitro-10H-acridin-9-one
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 60℃; for 0.5h; | 97% |
2-chloro-N-phenyl-9H-purin-6-amine
diethylaminopropylamine
2-(N,N-diethylamino-3-propylamino)-6-phenylamino-purine
Conditions | Yield |
---|---|
at 110℃; for 17h; | 97% |
Sulindac
diethylaminopropylamine
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In acetonitrile at 20℃; Inert atmosphere; | 97% |
4-(2-methyl-4-nitrophenoxy)pyridin-2-amine
diethylaminopropylamine
1-(3-diethylaminopropyl)-3-[4-(2-methyl-4-nitrophenoxy)pyridin-2-yl]urea
Conditions | Yield |
---|---|
Stage #1: 4-(2-methyl-4-nitrophenoxy)pyridin-2-amine; phenyl chloroformate With triethylamine In tetrahydrofuran at 0℃; for 0.5h; Stage #2: diethylaminopropylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 96.9% |
methyl 3,5-dimethoxybenzoate
diethylaminopropylamine
methyl 1-(2-bromoethyl)-3,5-dimethoxycyclohexa-2,5-diene-1-carboxylate
Conditions | Yield |
---|---|
Stage #1: methyl 3,5-dimethoxybenzoate With ammonia; lithium; tert-butyl alcohol In tetrahydrofuran at -78℃; Birch reduction alkylation; Stage #2: diethylaminopropylamine In tetrahydrofuran | 96% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 0.5h; | 96% |
In methanol at 20℃; for 72h; | 86% |
Conditions | Yield |
---|---|
Stage #1: ortho-nitrofluorobenzene; diethylaminopropylamine Stage #2: With hydrogenchloride In isopropyl alcohol | 96% |
benzo[b]thiophene-3-carbonyl azide
diethylaminopropylamine
Conditions | Yield |
---|---|
In benzene Heating; | 95% |
1-(chloro(piperidin-1-yl)methylene)piperidin-1-ium chloride
diethylaminopropylamine
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Inert atmosphere; Reflux; | 95% |
N,N,N',N'-tetramethylchlorformamidinium chloride
diethylaminopropylamine
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Inert atmosphere; Reflux; | 95% |
With triethylamine In acetonitrile at 0 - 80℃; for 5h; Inert atmosphere; Schlenk technique; |
diethylaminopropylamine
4-(3,3,4,4,5,5,5-heptafluoro-2,2-bis(trifluoromethyl)pentyl)benzoic acid
Conditions | Yield |
---|---|
Stage #1: 4-(3,3,4,4,5,5,5-heptafluoro-2,2-bis(trifluoromethyl)pentyl)benzoic acid With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 0.166667h; Cooling; Stage #2: diethylaminopropylamine In dichloromethane at 20℃; for 5h; | 95% |
Stage #1: 4-(3,3,4,4,5,5,5-heptafluoro-2,2-bis(trifluoromethyl)pentyl)benzoic acid With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 0.166667h; Stage #2: diethylaminopropylamine In dichloromethane at 20℃; for 5h; | 91% |
N-Methylisatoic anhydride
diethylaminopropylamine
N-Methyl-N'-(3-diethylaminopropyl)anthranilic amide
Conditions | Yield |
---|---|
In 1,4-dioxane at 70℃; for 8h; | 94% |
diethylaminopropylamine
3-(2,6-dichlorophenyl)-7-fluoro-1-methyl-1,6-naphthyridin-2(1H)-one
Conditions | Yield |
---|---|
In various solvent(s) for 17h; Amination; Heating; | 94% |
ethyl 2-isothiocyanatoacetate
diethylaminopropylamine
Conditions | Yield |
---|---|
In Petroleum ether for 4h; | 94% |
diethylaminopropylamine
N-(3-(diethylamino)propyl)-9-bromo-5,12-dioxo-5,12-dihydroindolizino[2,3-g]quinoline-6-carboxamide
Conditions | Yield |
---|---|
With dmap In chloroform for 5h; Reflux; | 94% |
N,N,N′,N′-tetraethylchloroformamidinium chloride
diethylaminopropylamine
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Inert atmosphere; Reflux; | 94% |
With triethylamine In acetonitrile at 0 - 80℃; for 5h; Inert atmosphere; Schlenk technique; |
6,7-difluoro-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one
diethylaminopropylamine
Conditions | Yield |
---|---|
at 100℃; for 12h; Sealed tube; | 94% |
at 100℃; for 12h; Sealed tube; | 74% |
With sodium carbonate In N,N-dimethyl-formamide at 140℃; for 2h; regioselective reaction; | 71% |
3-fluoro-6-nitrotoluene
diethylaminopropylamine
N1,N1-diethyl-N3-(3-methyl-4-nitrophenyl)-1,3-propanediamine
Conditions | Yield |
---|---|
With pyridine; sodium hydrogencarbonate for 3h; Heating; | 93% |
Product Name:3-Diethylaminopropylamine
The MF of 3-Diethylaminopropylamine(104-78-9) is C7H18N2.
The MW of 3-Diethylaminopropylamine(104-78-9) is 130.23.
Synonyms:1-(Diethylamino)propylamine-3;1,3-Propanediamine,N,N-diethyl-;3-(N,N-Diethylamino)-1-propylamine;N-(3-Diethylaminopropyl)amine;3-Propanediamine,N,N-diethyl-1;Diethylaminotrimethylenamine;N,N-(Diethylamino)propylamine
EINECS: 203-236-4
Mol File: 104-78-9.mol
Surface Tension: 30.8 dyne/cm
Density: 0.84 g/ml
Flash Point: 58.9 °C
Enthalpy of Vaporization: 40.71 kJ/mol
Boiling Point: 170.7 °C at 760 mmHg
Vapour Pressure: 1.45 mmHg at 25°C
Water Solubility: MISCIBLE
Sensitive: Air Sensitive
BRN: 741879
CAS DataBase Reference: 104-78-9(CAS DataBase Reference)
NIST Chemistry Reference: 104-78-9(NIST)
EPA Substance Registry System: 104-78-9(EPA Substance)
1. | skn-rbt 100 µg/24H open | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
2. | orl-rat LD50:1410 mg/kg | UCDS** Union Carbide Data Sheet. (Industrial Medicine and Toxicology Dept., Union Carbide Corp., 270 Park Ave., New York, NY 10017) 2/27 ,1967. | ||
3. | skn-rbt LD50:750 mg/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. |
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