N-(2-chlorophenyl)acetamide
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
In dichloromethane for 7h; Reflux; | 92% |
N-(2-chlorophenyl)acetamide
N,N-dimethyl-formamide
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With Triton X-100; trichlorophosphate In acetonitrile for 1.41667h; Vilsmeier-Haack cyclisation; Heating; | 88% |
With trichlorophosphate at 80 - 100℃; |
formic acid ethyl ester
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -78 - 0℃; for 3h; Stage #2: formic acid ethyl ester In tetrahydrofuran; hexane at -78℃; for 1h; |
2,8-dichloroquinoline
formic acid ethyl ester
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline With lithium diisopropyl amide In tetrahydrofuran; cyclohexene at -78℃; for 2h; Stage #2: formic acid ethyl ester In tetrahydrofuran; cyclohexene at -78℃; for 4h; |
2-Chloroaniline
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride / water 2: trichlorophosphate / 80 - 100 °C View Scheme |
4-morpholinecarboxaldehyde
2,8-dichloroquinoline
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine; n-butyllithium In 2-methyltetrahydrofuran; hexane at -78 - -70℃; |
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(pyrazin-2-yl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane at 110℃; for 5h; Inert atmosphere; | 99% |
(R)-2-methylpropane-2-sulfinamide
2,8-dichloroquinoline-3-carbaldehyde
(R,E)-N-[(2, 8-dichloroquinolin-3-yl)methylidene]-2-methylpropane-2-sulfinamide
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 0.25h; Stage #2: (R)-2-methylpropane-2-sulfinamide at 20℃; for 17h; | 97% |
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 0.25h; Stage #2: (R)-2-methylpropane-2-sulfinamide In tetrahydrofuran at 20℃; for 17h; | 97% |
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 0.25h; Stage #2: (R)-2-methylpropane-2-sulfinamide In tetrahydrofuran at 20℃; for 17h; | 97% |
2,8-dichloroquinoline-3-carbaldehyde
phenylboronic acid
8-chloro-2-phenylquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In 1,2-dimethoxyethane; water at 110℃; for 4h; Suzuki Coupling; Inert atmosphere; | 97% |
2,8-dichloroquinoline-3-carbaldehyde
(S)-2-methylpropane-2-sulfinamide
2-methylpropane-2(S)-sulfinic acid N-(2,8-dichloroquinolin-3-yl)meth-(E)-ylideneamide
Conditions | Yield |
---|---|
Stage #1: (S)-2-methylpropane-2-sulfinamide With potassium phosphate In water for 0.166667h; Stage #2: 2,8-dichloroquinoline-3-carbaldehyde In water; isopropyl alcohol for 48h; | 95% |
3-pyridylboronic acid
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(pyridin-3-yl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In 1,2-dimethoxyethane; water at 90℃; for 7h; Suzuki Coupling; Inert atmosphere; | 91% |
With tris-(dibenzylideneacetone)dipalladium(0); triethylamine; tri tert-butylphosphoniumtetrafluoroborate In ethanol; water at 70℃; Inert atmosphere; |
(R)-2-methylpropane-2-sulfinamide
2,8-dichloroquinoline-3-carbaldehyde
N-[(2,8-dichloroquinolin-3-yl)methylene]-2-methylpropane-2(R)-sulfinamide
Conditions | Yield |
---|---|
titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 17.25h; Inert atmosphere; | 89% |
4,6-dihydroxy-2-mercaptopyrimidine
Chloroacetic anhydride
2,8-dichloroquinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With copper In ethanol for 1h; Irradiation; | 89% |
2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(2-methylpyridin-3-yl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; for 3h; | 86.43% |
o-fluorophenylboronic acid
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(2-fluorophenyl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; for 1h; | 83.1% |
4-cyclohexyl-thiosemicarbazide
2,8-dichloroquinoline-3-carbaldehyde
1-((2,8-dichloroquinolin-3-yl)methylene)-4-cyclohexylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 4-cyclohexyl-thiosemicarbazide; 2,8-dichloroquinoline-3-carbaldehyde In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 81% |
thiosemicarbazide
2,8-dichloroquinoline-3-carbaldehyde
1-((2,8-dichloroquinolin-3-yl)methylene)thiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: thiosemicarbazide; 2,8-dichloroquinoline-3-carbaldehyde In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 79% |
2,8-dichloroquinoline-3-carbaldehyde
4-(4-methylphenyl)-3-thiosemicarbazide
1-((2,8-dichloroquinolin-3-yl)methylene)-4-p-tolylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde; 4-(4-methylphenyl)-3-thiosemicarbazide In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 76% |
2,8-dichloroquinoline-3-carbaldehyde
4-cyclopentyl thiosemicarbazide
1-((2,8-dichloroquinolin-3-yl)methylene)-4-cyclopentylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde; 4-cyclopentyl thiosemicarbazide In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 76% |
2,8-dichloroquinoline-3-carbaldehyde
2-trifluoromethoxyphenylboronic acid
8-chloro-2-(2-(trifluoromethoxy)phenyl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; for 15h; | 70.9% |
2,8-dichloroquinoline-3-carbaldehyde
6-chloropyridin-3-ylboronic acid
8-chloro-2-(6-chloropyridin-3-yl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane; water at 90℃; for 16h; Suzuki Coupling; Inert atmosphere; | 70% |
2,8-dichloroquinoline-3-carbaldehyde
4-(2-methylphenyl)-3-thiosemicarbazide
1-((2,8-dichloroquinolin-3-yl)methylene)-4-o-tolylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde; 4-(2-methylphenyl)-3-thiosemicarbazide In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 69% |
4-(4-nitrophenyl)-3-thiosemicarbazide
2,8-dichloroquinoline-3-carbaldehyde
1-((2,8-dichloroquinolin-3-yl)methylene)-4-p-nitrophenylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 4-(4-nitrophenyl)-3-thiosemicarbazide; 2,8-dichloroquinoline-3-carbaldehyde In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 67% |
2-methoxy-6-(tri-n-butylstannyl)pyrazine
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(6-methoxypyrazin-2-yl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane at 110℃; Inert atmosphere; | 63% |
2,8-dichloroquinoline-3-carbaldehyde
C8H15NHCSNHNH2
1-((2,8-dichloroquinolin-3-yl)methylene)-4-cyclooctylthiosemicarbazide
Conditions | Yield |
---|---|
Stage #1: 2,8-dichloroquinoline-3-carbaldehyde; C8H15NHCSNHNH2 In ethanol Stage #2: With acetic acid In ethanol at 60℃; for 12h; | 62% |
(5-fluoro-2-(trifluoromethyl)phenyl)boronic acid
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(5-fluoro-2-(trifluoromethyl)phenyl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; for 14h; | 19.4% |
2-(trifluoromethyl)phenylboronic acid
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(2-(trifluoromethyl)phenyl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; |
(5-fluoro-2-methoxyphenyl)boronic acid
2,8-dichloroquinoline-3-carbaldehyde
8-chloro-2-(5-fluoro-2-methoxyphenyl)quinoline-3-carbaldehyde
Conditions | Yield |
---|---|
With sodium carbonate; tetrakis(triphenylphosphine) palladium(0) In water; acetonitrile at 100℃; for 4h; |
2,8-dichloroquinoline-3-carbaldehyde
(S)-tert-butyl 1-(2,8-dichloroquinolin-3-yl)ethylcarbarnate
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: Cooling with ice 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 20 °C 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: titanium(IV)isopropoxide / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C / Inert atmosphere 1.2: 17 h / 20 °C / Inert atmosphere 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: cooling with ice-salt 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 20 °C / Inert atmosphere 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere View Scheme |
2,8-dichloroquinoline-3-carbaldehyde
(R)-N-[(S)-1-(2,8-dichloroquinolin-3-yl)ethyl]-2-methylpropane-2-sulfinamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: Cooling with ice View Scheme | |
Multi-step reaction with 2 steps 1.1: titanium(IV)isopropoxide / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C / Inert atmosphere 1.2: 17 h / 20 °C / Inert atmosphere 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: cooling with ice-salt View Scheme |
2,8-dichloroquinoline-3-carbaldehyde
(S)-1-(2,8-dichloroquinolin-3-yl)ethanamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: Cooling with ice 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: titanium(IV)isopropoxide / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h View Scheme | |
Multi-step reaction with 3 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C / Inert atmosphere 1.2: 17 h / 20 °C / Inert atmosphere 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: cooling with ice-salt 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 20 °C / Inert atmosphere View Scheme |
2,8-dichloroquinoline-3-carbaldehyde
C23H32ClN5O3
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: titanium(IV) isopropylate / tetrahydrofuran / 0.25 h / 20 °C 1.2: 17 h / 20 °C 2.1: dichloromethane; diethyl ether / -70 - 20 °C / Inert atmosphere 2.2: Cooling with ice 3.1: hydrogenchloride / 1,4-dioxane; methanol / 2 h / 20 °C 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C 5.1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 2 h / 130 °C / microwave irradiation View Scheme |
The 2,8-Dichloroquinoline-3-carboxaldehyde has the CAS registry number 144918-96-7. This chemical's molecular formula is C10H5Cl2NO and molecular weight is 226.06. What's more, its systematic name is 2,8-dichloroquinoline-3-carbaldehyde.
Physical properties of 2,8-Dichloroquinoline-3-carboxaldehyde are: (1)ACD/LogP: 3.07; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.07; (4)ACD/LogD (pH 7.4): 3.07; (5)ACD/BCF (pH 5.5): 127.31; (6)ACD/BCF (pH 7.4): 127.31; (7)ACD/KOC (pH 5.5): 1117.57; (8)ACD/KOC (pH 7.4): 1117.57; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 29.96 Å2; (13)Index of Refraction: 1.697 ; (14)Molar Refractivity: 58.72 cm3; (15)Molar Volume: 152.3 cm3; (16)Polarizability: 23.28×10-24cm3; (17)Surface Tension: 58.9 dyne/cm; (18)Density: 1.483 g/cm3; (19)Flash Point: 170.4 °C; (20)Enthalpy of Vaporization: 60.35 kJ/mol; (21)Boiling Point: 358.1 °C at 760 mmHg; (22)Vapour Pressure: 2.61E-05 mmHg at 25°C.
Preparation of 2,8-Dichloroquinoline-3-carboxaldehyde: this chemical can be prepared by N,N-dimethyl-formamide and acetic acid-(2-chloro-anilide) by heating. This reaction will need reagents POCl3, Triton X-100 and solvent acetonitrile with the reaction time of 85 min. The yield is about 88%.
You can still convert the following datas into molecular structure:
(1)SMILES: Clc1cccc2cc(C=O)c(Cl)nc12
(2)InChI: InChI=1S/C10H5Cl2NO/c11-8-3-1-2-6-4-7(5-14)10(12)13-9(6)8/h1-5H
(3)InChIKey: LPMXEZKNTOGEMM-UHFFFAOYSA-N
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