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inquiryProduct name: 4-(3,4-Dichlorophenyl)-1,2,3,4-Tetrahydro-N-Methyl-1-Naphthalenimine CAS No.:79560-20-6 Molecule Formula:C17H15Cl2N Molecule Weight:304.21 Purity: 97.0% Package: 25kg/drum Description:White or almost white crystalline powd
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inquiryN-(4(3,4-dichlorophenyl)-3,4-dihydro-1(2H)naphthalidene) met...Appearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air
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inquiry4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one
methylamine
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
In ethanol at 0℃; Solvent; Heating; Industrial scale; Large scale; | 95% |
With formic acid In methanol | 95% |
With thionyl chloride In tetrahydrofuran at -10 - 20℃; | 93% |
4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one
methylamine
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
methanesulfonic acid In ethanol at 0 - 70℃; for 4h; | 88% |
methanesulfonic acid In acetonitrile at 0 - 70℃; for 4h; | 88% |
In triethylamine at 0 - 90℃; for 10h; | 87% |
toluene-4-sulfonic acid In triethylamine at 0 - 50℃; for 4h; | 82% |
3,4-dichlorobenzophenone
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: potassium tert-butoxide / 2-methyl-propan-2-ol / 16 h / Heating 2: 50 percent / 48percent aq. HBr / acetic acid / 36 h / Heating 3: 100 percent / H2 / 5percent Pd/C / ethyl acetate / 24 h / 760 Torr / Ambient temperature 4: SOCl2 / toluene / 1.25 h 5: AlCl3 / CS2 / 16 h / Ambient temperature 6: TiCl4 / toluene / 17 h / Ambient temperature View Scheme |
4-(3,4-dichlorophenyl)-4-phenylbutanoic acid
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: SOCl2 / toluene / 1.25 h 2: AlCl3 / CS2 / 16 h / Ambient temperature 3: TiCl4 / toluene / 17 h / Ambient temperature View Scheme |
4-(3,4-dichlorophenyl)-4-phenylbut-3-enoic acid
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 100 percent / H2 / 5percent Pd/C / ethyl acetate / 24 h / 760 Torr / Ambient temperature 2: SOCl2 / toluene / 1.25 h 3: AlCl3 / CS2 / 16 h / Ambient temperature 4: TiCl4 / toluene / 17 h / Ambient temperature View Scheme |
4-(3,4-dichlorophenyl)-4-phenylbutyric acid
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 / CS2 / 16 h / Ambient temperature 2: TiCl4 / toluene / 17 h / Ambient temperature View Scheme |
3-(ethoxycarbonyl)-4-(3,4-dichlorophenyl)-4-phenylbut-3-enoic acid
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 50 percent / 48percent aq. HBr / acetic acid / 36 h / Heating 2: 100 percent / H2 / 5percent Pd/C / ethyl acetate / 24 h / 760 Torr / Ambient temperature 3: SOCl2 / toluene / 1.25 h 4: AlCl3 / CS2 / 16 h / Ambient temperature 5: TiCl4 / toluene / 17 h / Ambient temperature View Scheme |
4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one
methylamine
A
2,3-dichlorosertraline-imine
B
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
methanesulfonic acid In ethanol at 0 - 70℃; for 4h; | |
toluene-4-sulfonic acid at 60℃; under 3750.38 - 7500.75 Torr; for 5h; |
4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
With formic acid; methylamine In N,N-dimethyl-formamide |
1,2-dichloro-benzene
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aluminum (III) chloride 2: ethanol / 0 °C / Heating; Industrial scale; Large scale View Scheme |
α-naphthol
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aluminum (III) chloride 2: ethanol / 0 °C / Heating; Industrial scale; Large scale View Scheme |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
With hydrogen; 5 % alumina-supported palladium In methanol at 26 - 29℃; Product distribution / selectivity; Autoclave; | A 91.52% B 6.54% |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Conditions | Yield |
---|---|
With hydrogen; CuCrBa oxide In ethanol at 130 - 150℃; under 9000.9 Torr; for 1h; | 83% |
With hydrogen; CuCrBa oxide In butan-1-ol | |
With hydrogen; CuCrBa oxide In isopropyl alcohol | |
With hydrogen; CuCrBa oxide In methanol |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
sertraline
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate; 1,1'-[1-methyl-3-(2,6-dimethylpiperidinyl)-1,3-propyl]ferrocene; hydrogen In toluene at 80℃; under 15001.5 Torr; | 83% |
With tris(pentafluorophenyl)borate; diisopropylamine at 100℃; for 24h; Neat (no solvent); | 90 %Spectr. |
With 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; tert-butyl alcohol In chloroform-d1 | 83 %Spectr. |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
cis-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthaleneamine
trans-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol for 1.5h; Ambient temperature; | |
With palladium on activated charcoal; hydrogen | A n/a B n/a |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
cis-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthaleneamine
Conditions | Yield |
---|---|
With hydrogen; 5 wt% palladium on calcium carbonate In methanol; water at 20 - 35℃; for 3.5h; | |
With Lindlar's catalyst; hydrogen; pyrographite In ethanol at 20 - 40℃; Solvent; Industrial scale; Large scale; | n/a |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
(1R,4R)-sertraline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium borohydride / methanol / 1.5 h / Ambient temperature View Scheme |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
trans-(1S,4R)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium borohydride / methanol / 1.5 h / Ambient temperature View Scheme |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
trans-(1R,4S)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium borohydride / methanol / 1.5 h / Ambient temperature View Scheme |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
Sertraline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium borohydride / methanol / 1.5 h / Ambient temperature View Scheme | |
Stage #1: With hydrogen; G-69 (Ni/Kieselguhr) at 150℃; for 2h; Stage #2: N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine With hydrogen In tetrahydrofuran at 90℃; under 6080.41 Torr; | 86 %Chromat. |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
A
cis-(1S,4S)-N-methyl-(3-chlorophenyl)-1,2,3,4-tetrahydro-1-naphtalenamine
B
(1S)-cis-N-methyl-4-(4-chlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
C
4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one
D
trans-(1S,4R)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
E
Sertraline
Conditions | Yield |
---|---|
With hydrogen; SA-3135 support, Co(NO3)2, H2O; dried and calcined ones or twice (Co 11 - 25percent); reduction with H2 In tetrahydrofuran at 120 - 150℃; under 6000.6 Torr; | A n/a B n/a C 0.2 - 0.7 %Chromat. D 7 - 9.4 %Chromat. E 87 - 91 %Chromat. |
triphenyl phosphite
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
sertraline
Conditions | Yield |
---|---|
palladium on graphite In N-methyl-acetamide; methanol |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
sertraline
Conditions | Yield |
---|---|
With phosphorous acid trimethyl ester In methanol |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
B
sertraline hydrochloride
Conditions | Yield |
---|---|
Stage #1: N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine With hydrogen; pyridine hydrochloride; 50% Pd/C In methanol at 25 - 35℃; for 6h; Stage #2: With hydrogenchloride In methanol; water pH=1 - 2; Product distribution / selectivity; | |
Stage #1: N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine With hydrogen; pyridine hydrochloride; platinum on carbon In methanol at 25 - 35℃; for 0.5h; Stage #2: With hydrogenchloride In methanol; water pH=1 - 2; Product distribution / selectivity; | |
Stage #1: N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine With hydrogen; N,N-dimethylacetamide hydrochloride; 50% Pd/C In methanol at 25 - 35℃; for 4h; Stage #2: With hydrogenchloride In methanol; water pH=1 - 2; Product distribution / selectivity; |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
A
(1R,4R)-sertraline
B
trans-(1S,4R)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
C
trans-(1R,4S)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
D
Sertraline
Conditions | Yield |
---|---|
With C32H12BF24(1-)*C36H44IrNOP(1+); hydrogen at 20℃; under 15201 Torr; for 12h; optical yield given as %ee; enantioselective reaction; |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
A
(1R,4R)-sertraline
B
trans-(1R,4S)-N-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenamine
C
Sertraline
Conditions | Yield |
---|---|
With R,S-[Ir(1,5-cyclooctadiene)(PPh2(C9H10)(C3H3NO-i-Bu))] tetrakis(3,5-bis(trifluoromethyl)phenyl)borate; hydrogen at 20℃; under 15201 Torr; for 12h; optical yield given as %ee; enantioselective reaction; |
N-[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene]methanamine
(cis-1S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine (R)-mandelate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyrographite; hydrogen; Lindlar's catalyst / ethanol / 20 - 40 °C / Industrial scale; Large scale 2: ethanol / Reflux; Industrial scale; Large scale View Scheme |
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