2-<2-(Methylthio)propyl>-1H-isoindole-1,3(2H)-dione
3-methylthio-1-propanamine
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 1h; Wavelength; Microwave irradiation; Sonication; Reflux; | 87.5% |
With ethanol; hydrazine hydrate | |
With hydrazine |
Conditions | Yield |
---|---|
cyclohexenone In various solvent(s) at 154℃; for 2h; | 72.8% |
With cyclohexenone In cyclohexanol for 5h; Heating; | |
With 3,5,5-Trimethylcyclohex-2-en-1-one In isopropyl alcohol at 150℃; for 4h; Autoclave; | 90 %Chromat. |
2-<2-(Methylthio)propyl>-1H-isoindole-1,3(2H)-dione
3-methylthio-1-propanamine
Conditions | Yield |
---|---|
anschliessende Behandlung mit Salzsaeure; |
3-(methylthio)propionitrile
3-methylthio-1-propanamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether | |
With lithium aluminium tetrahydride In diethyl ether | |
With lithium aluminium tetrahydride | |
With sodium tetrahydroborate; nickel dichloride In N,N-dimethyl-formamide at 20℃; |
Conditions | Yield |
---|---|
With nitrobenzene; 4-dimethylamino-benzaldehyde at 150 - 190℃; | |
With paraffin at 250℃; | |
With cyclohexenone In cyclohexanol for 5h; Heating; | |
With 1,10-Phenanthroline; copper hydroxide In 1-methyl-pyrrolidin-2-one at 210℃; for 4h; Inert atmosphere; Green chemistry; |
Conditions | Yield |
---|---|
In water Rate constant; pH=8.3; |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
at 250℃; (+-)-2-amino-4-methylsulfanyl-butyric acid; |
3-methylthio-1-propanamine
Conditions | Yield |
---|---|
With sodium hydroxide folgende Behandlung mit Salzsaeure; |
DL-methionine
A
3-methylthio-1-propanamine
B
3-(methylsulfenyl)propanal
C
methionine S-oxide
D
2-aminobutanoic acid
Conditions | Yield |
---|---|
With water; dinitrogen monoxide Mechanism; Quantum yield; γ-irradiation; |
3-methylthio-1-propanamine
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-formamide With bis(2-chlorophenyl)borinic acid; acetic acid at 20℃; for 0.25h; Inert atmosphere; Stage #2: 3-methylthio-1-propanamine at 20℃; for 72h; Inert atmosphere; | 99% |
3-methylthio-1-propanamine
methyl 4-[(4-phenyl)thiazol-2-yl]benzoate
methyl 3-{4-[(4-phenyl)thiazol-2-yl]benzamido}propyl sulfide
Conditions | Yield |
---|---|
at 70 - 75℃; aminolysis; | 98% |
3-methylthio-1-propanamine
chloro-diphenylphosphine
bis(diphenylphosphino)(N-(methylthio)propyl)amine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 97% |
With triethylamine In dichloromethane at 20℃; for 20h; | 97% |
methyl 2'-phenyl-2,4'-bithiazole-4-carboxylate
3-methylthio-1-propanamine
methyl 3-(2'-phenyl-2,4'-bithiazole-4-carboxamido)propyl sulfide
Conditions | Yield |
---|---|
at 80℃; for 2h; | 96% |
3-methylthio-1-propanamine
3-bromo-6-chloro-imidazo[1,2-b]pyridazine
C10H13BrN4S
Conditions | Yield |
---|---|
With triethylamine In 1-methyl-pyrrolidin-2-one at 125 - 140℃; | 96% |
5-[(2,5-difluorophenyl)[(4-fluorophenyl)sulfonyl]methyl]-4-methylpyridine-2-carboxylic acid
3-methylthio-1-propanamine
5-[(2,5-difluorophenyl)[(4-fluorophenyl)sulfonyl]methyl]-4-methyl-N-[3-(methylthio)propyl]pyridine-2-carboxamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 72h; | 94% |
3-methylthio-1-propanamine
2-amino-5-hydroxy-[1,4]benzoquinone-4-imine
Conditions | Yield |
---|---|
In ethanol for 2h; Reflux; | 94% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 72h; Reflux; | 93.8% |
3-methylthio-1-propanamine
2-3'-2''-acetoxy-2'',3'',-dihydrofur-4''-ylacrylamido-3-hydroxy-2-cyclopenten-1-one
A
reductiline
Conditions | Yield |
---|---|
for 17h; Ambient temperature; | A 92% B n/a |
3-methylthio-1-propanamine
methyl 2''-phenyl-2,4':2',4''-terthiazole-4-carboxylate
methyl 3-(2''-phenyl-2,4':2',4''-terthiazole-4-carboxamido)propyl sulfide
Conditions | Yield |
---|---|
at 60 - 70℃; for 6h; | 92% |
3-methylthio-1-propanamine
S-phenyl thiopantothenate
N-(3-(methylthio)-propyl) pantothenamide
Conditions | Yield |
---|---|
In acetonitrile at 30℃; for 3h; | 92% |
3-methylthio-1-propanamine
4,6-diaminoresorcin dihydrochloride
Conditions | Yield |
---|---|
In ethanol; water at 20℃; for 2h; | 92% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 1h; | 91% |
3-methylthio-1-propanamine
N-(tert-butoxycarbonyl)-S-methyl-L-cysteine
N-(tert-butoxycarbonyl)-S-methyl-(S)-cysteine <3-(methylthio)propyl>amide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In acetonitrile for 72h; Ambient temperature; | 90% |
3-methylthio-1-propanamine
2'-<2-(trifluoroacetamido)ethyl>-2,4'-bithiazole-4-carboxylic acid
methyl 3-<2'-<2-(trifluoroacetamido)ethyl>-2,4'-bithiazole-4-carboxamido>propyl sulfide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride | 90% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran; N,N-dimethyl-formamide at 25℃; for 14h; | 90% |
3-methylthio-1-propanamine
2-Bromoacetyl bromide
N-(3-(methylthio)propyl)-2-(3-(methylthio)propylamino)acetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -78 - 20℃; | 89% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 96h; | 89% |
3-methylthio-1-propanamine
2'-(2-benzyloxy-ethyl)-[2,4']bithiazolyl-4-carboxylic acid
2'-(2-benzyloxy-ethyl)-[2,4']bithiazolyl-4-carboxylic acid (3-methylsulfanyl-propyl)-amide
Conditions | Yield |
---|---|
With 1-hydroxy-7-aza-benzotriazole; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0 - 25℃; | 88% |
Conditions | Yield |
---|---|
In methanol; water at 20℃; for 1.5h; Inert atmosphere; | 88% |
3-methylthio-1-propanamine
homopantothenic acid phenyl thioester
Conditions | Yield |
---|---|
In acetonitrile at 30℃; for 3h; | 87% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 24h; Cooling with ice; | 87% |
Conditions | Yield |
---|---|
Stage #1: hydrogenchloride; 3-methylthio-1-propanamine In dichloromethane; water Inert atmosphere; Schlenk technique; Stage #2: cobalt(II) chloride In dichloromethane; water for 2h; Schlenk technique; Inert atmosphere; | 86% |
3-methylthio-1-propanamine
S-phenyl thio-α-pantothenate
N-(3-(methylthio)-propyl) α-pantothenamide
Conditions | Yield |
---|---|
In acetonitrile at 30℃; for 3h; | 85% |
3-methylthio-1-propanamine
4-(cyclopropylethynyl)-N-(3-formyl-8-methylquinolin-7-yl)benzamide
4-(cyclopropylethynyl)-N-[8-methyl-3-({[3-(methylthio)propyl]amino}methyl)quinolin-7-yl]benzamide
Conditions | Yield |
---|---|
Stage #1: 3-methylthio-1-propanamine; 4-(cyclopropylethynyl)-N-(3-formyl-8-methylquinolin-7-yl)benzamide With acetic acid In N,N-dimethyl acetamide at 15 - 30℃; for 0.166667h; Stage #2: With sodium tris(acetoxy)borohydride; acetic acid In N,N-dimethyl acetamide at 5 - 30℃; Stage #3: With sodium hydroxide In N,N-dimethyl acetamide; water at 5℃; | 85% |
3-methylthio-1-propanamine
2-((2RS,3RS)-3-ethyloxiran-2-yl)ethan-1-ol
Conditions | Yield |
---|---|
Stage #1: 2-((2RS,3RS)-3-ethyloxiran-2-yl)ethan-1-ol With methanesulfonyl chloride; triethylamine In dichloromethane at 0 - 20℃; for 0.166667h; Inert atmosphere; Stage #2: 3-methylthio-1-propanamine With sodium iodide In dimethyl sulfoxide at 20℃; for 48h; Inert atmosphere; | 85% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 84% |
With triethylamine In dichloromethane at 20℃; for 20h; | 84% |
4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline
3-methylthio-1-propanamine
1-(2,8-bis(trifluoromethyl)quinolin-4-yl)-2-(3-(methylthio)propylamino)ethanol
Conditions | Yield |
---|---|
In ethanol at 130℃; under 14221.9 Torr; Microwave irradiation; | 84% |
3-methylthio-1-propanamine
1-tert-butoxycarbonyl-3,4-epoxypyrrolidine
Conditions | Yield |
---|---|
In ethanol Heating; | 83.5% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 83.4% |
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