As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryChlorpromazine CAS:50-53-3 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates
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inquiryChlorpromazine CAS 50-53-3 Purity: 99% Min Application: Intermediates Appearance: Powder Package: Bag Delivery: 3-5days Our Advantage & Service 1.Top quality: Using high quality material and establishing a strict quality control syst
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Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
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inquiryC11H16ClIN2
2-bromothiophenol
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With copper(l) iodide; potassium carbonate; L-proline In ethyl methyl ether at 90 - 110℃; Inert atmosphere; | 78% |
formaldehyd
2-chloro-10-(3-aminopropyl)phenothiazine
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With formic acid In water at 80℃; for 8h; Eschweiler-Clark Amine Methylation; Microwave irradiation; | 66% |
2-bromo-4-chloroiodobenzene
2-bromothiophenol
1-amino-3-(dimethylamino)propane
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate In toluene at 60 - 160℃; for 2.33333h; Microwave irradiation; | 50% |
2-chlorophenothiazine
3-(Dimethylamino)propyl chloride
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With sodium amide | |
(i) NaNH2, toluene, (ii) /BRN= 605294/; Multistep reaction; | |
With potassium hydroxide; potassium carbonate; tetra(n-butyl)ammonium hydrogensulfate toluene 1.) room temp., 2 h, 2.) reflux, 18 h; Yield given. Multistep reaction; |
3-Dimethylamino-1-propanol
2-chloro-phenothiazine-10-carbonyl chloride
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With toluene Erhitzen des Reaktionsprodukts unter vermindertem Druck auf 210-220grad; |
3-(2-chloro-10H-phenothiazin-10-yl)propanonitrile
A
2-chloro-10-(3-aminopropyl)phenothiazine
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With nickel; dimethyl amine; benzene at 110 - 116℃; under 58840.6 Torr; Hydrogenation; |
N'-[2-(2-bromo-phenylsulfanyl)-5-chloro-phenyl]-N,N-dimethyl-propanediyldiamine
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With copper; potassium carbonate; N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
With iron; acetic acid; xylene |
1-(2-chloro-phenothiazin-10-yl)-3-methanesulfonyloxy-propane
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With dimethyl amine |
bis-[3-(2-chloro-phenothiazin-10-yl)-propyl]-methyl-amine
A
10-Allyl-2-chlorophenothiazine
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With sodium hydroxide; methyl iodide |
2-chloro-10-(3-chloropropyl)-10H-phenothiazine
dimethyl amine
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In ethanol |
dopamine
chloropromazine cation radical
A
dopaminoquinone
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In hydrogenchloride Rate constant; pH=1.5; |
2-chlorophenothiazine
3-(Dimethylamino)propyl chloride
A
2-chloro-10-methyl-10H-phenothiazine
B
10-Allyl-2-chlorophenothiazine
C
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With sodium hydroxide In chlorobenzene; toluene for 4.5h; Heating; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride 1.) THF, -45 deg C - 60 deg C, 2.) 60 deg C, 10 min; Yield given. Multistep reaction; |
Norepinephrine
chloropromazine cation radical
A
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
B
4-(2-Amino-1-hydroxy-ethyl)-[1,2]benzoquinone
Conditions | Yield |
---|---|
In hydrogenchloride Rate constant; pH=7; |
Epinephrine
chloropromazine cation radical
A
adrenaline o-quinone
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In hydrogenchloride Rate constant; pH=7; |
aminopyrine
A
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
B
aminopyrine radical cation
Conditions | Yield |
---|---|
Rate constant; pH 6; |
[3-(2-Chloro-phenothiazin-10-yl)-propyl]-dimethyl-(2-methyl-acryloyloxymethyl)-ammonium; chloride
A
formaldehyd
B
poly(methacrylic acid)
C
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In water at 21℃; pH=8.8, ionic strength 0.1 M KCl; other pH, other temp.; hydrolysis rate; |
Benzoyloxymethyl-[3-(2-chloro-phenothiazin-10-yl)-propyl]-dimethyl-ammonium; chloride
A
formaldehyd
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
C
benzoic acid
Conditions | Yield |
---|---|
In water at 21℃; pH=8.2, ionic strength 0.1 M KCl; other pH; hydrolysis rate; |
dopamine
A
dopaminoquinone
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
Kinetics; Rate constant; in constant ionic strength (0.8 M) mixtures of HClO4 and NaClO4 in 40percent MeO/H2O (w/w) with a pH between 0.1 and 1.5; |
chloropromazine cation radical
4-methyl-1,2-dihydroxybenzene
A
4-methylbenzo-1,2-quinone
B
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In hydrogenchloride Rate constant; pH=7; |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With palladium on activated charcoal; acetic acid Hydrogenation; |
Conditions | Yield |
---|---|
With n-butyllithium; diethyl ether |
Conditions | Yield |
---|---|
With xylene |
2-chloro-N-methyl-10H-phenothiazine-10-propanamine hydrochloride
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (NH4)2SO4 / 110 °C 2: 2.) LiAlH4 / 1.) THF, -45 deg C - 60 deg C, 2.) 60 deg C, 10 min View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aqueous H2O2; ethanol 2: iron-powder; acetic acid; xylene View Scheme | |
With potassium carbonate In water pH=10; Inert atmosphere; |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In acetone at 40℃; for 48h; Inert atmosphere; Reflux; | 97% |
Conditions | Yield |
---|---|
With methanesulfonato(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-methylamino-1,1'-biphenyl-2-yl)palladium(II); potassium hydroxide In water; toluene at 110℃; Flow reactor; | 95% |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
With GLUTATHIONE; isopropyl alcohol; acetone In water Rate constant; Product distribution; Irradiation; pH=3; pulse radiolysis; other thiol reagents and CPZ concentrations; | 91% |
With halothane peroxyl radical In various solvent(s) Rate constant; Ambient temperature; Irradiation; pH=7; pulse radiolysis; different CZ concentrations; | 54 % Spectr. |
With dihydrogen peroxide; horseradish peroxidase In acetate buffer pH=4.5; Kinetics; Further Variations:; Reagents; Oxidation; | |
With hydroxyl pH=7; Kinetics; aq. phosphate buffer; |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
10-[3-(dimethylamino)propyl]-10H-phenothiazin-2-ol
Conditions | Yield |
---|---|
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; boric acid; palladium diacetate; caesium carbonate In 1-methyl-pyrrolidin-2-one at 100℃; for 14h; Schlenk technique; Inert atmosphere; | 87% |
With water for 120h; Irradiation; |
Conditions | Yield |
---|---|
In acetonitrile Electrolysis; | 83% |
With hydrogenchloride; sodium nitrite In water for 2h; Product distribution; oxidation of phenothiazine salts to their sulfoxides with aqueous nitrous acid; hydrogen peroxide oxidation; | 74% |
With hydrogenchloride; sodium nitrite In water for 2h; | 74% |
chloromethyl benzoate
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Benzoyloxymethyl-[3-(2-chloro-phenothiazin-10-yl)-propyl]-dimethyl-ammonium; chloride
Conditions | Yield |
---|---|
In acetone | 81.5% |
carbonochloridic acid 1-chloro-ethyl ester
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane for 1h; Substitution; Heating; | 81% |
Chloromethyl methacrylate
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
[3-(2-Chloro-phenothiazin-10-yl)-propyl]-dimethyl-(2-methyl-acryloyloxymethyl)-ammonium; chloride
Conditions | Yield |
---|---|
In acetone | 79% |
Conditions | Yield |
---|---|
With Cy-DHTP*HBF4; palladium diacetate; lithium tert-butoxide In toluene at 20 - 110℃; for 21h; Inert atmosphere; Sealed tube; | 65% |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester
chlorpromazine N+-glucuronide chloride
Conditions | Yield |
---|---|
With XAD-2 ion-exchange resin; sodium hydrogencarbonate In water; benzene for 72h; Ambient temperature; | 46% |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester
A
chlorpromazine N+-glucuronide chloride
B
[3-(2-Chloro-phenothiazin-10-yl)-propyl]-dimethyl-((2R,3R,4S,5S,6S)-3,4,5-triacetoxy-6-methoxycarbonyl-tetrahydro-pyran-2-yl)-ammonium; bromide
C
Hydrogen carbonate[3-(2-chloro-phenothiazin-10-yl)-propyl]-dimethyl-((2R,3R,4S,5S,6S)-3,4,5-triacetoxy-6-carboxy-tetrahydro-pyran-2-yl)-ammonium;
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; benzene for 72h; Ambient temperature; | A 46% B n/a C n/a |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
A
Chlorpromazine oxide
B
chlorpromazine sulfoxide
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid; sodium hydroxide In dichloromethane at 0℃; for 4h; | A 40% B 10% |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
A
7-hydroxychlorpromazine
B
2-chloro-10-(3-dimethylamino-propyl)-10H-phenothiazin-1-ol
C
3-hydroxyl CPZ
D
chlorpromazine sulfoxide
Conditions | Yield |
---|---|
Stage #1: 2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine With ethylenediaminetetraacetic acid trisodium salt; oxygen; manganese (II) acetate tetrahydrate; ascorbic acid In water pH=4; Udenfriend reaction; Stage #2: With ferrous(II) sulfate heptahydrate; ethylenediaminetetraacetic acid trisodium salt; oxygen In water at 45℃; for 2h; Udenfriend reaction; | A n/a B 0.4% C 0.84% D 0.58% |
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
chlorpromazine N',S-dioxide
Conditions | Yield |
---|---|
With ethanol; dihydrogen peroxide | |
With dihydrogen peroxide In ethanol | |
With dihydrogen peroxide In ethanol for 24h; Ambient temperature; | |
Multi-step reaction with 2 steps 1: aq. H2O2, NH3 / ethanol / 60 h 2: aq. H2O2 / ethanol / 84 h View Scheme | |
Multi-step reaction with 2 steps 1: 3-chloro-benzenecarboperoxoic acid; sodium hydroxide / dichloromethane / 4 h / 0 °C 2: 3-chloro-benzenecarboperoxoic acid; sodium hydroxide / dichloromethane / 4 h / 0 °C View Scheme |
9-(bromomethyl)acridine
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
acridin-9-ylmethyl-[3-(2-chloro-phenothiazin-10-yl)-propyl]-dimethyl-ammonium; bromide
Conditions | Yield |
---|---|
In acetonitrile Ambient temperature; |
2-bromo-1-phenyl-ethanone oxime
2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine
[3-(2-chloro-phenothiazin-10-yl)-propyl]-(2-hydroxyimino-2-phenyl-ethyl)-dimethyl-ammonium; bromide
Conditions | Yield |
---|---|
In diethyl ether |