2-methoxy-5-(methylsulfonyl)aniline
1-hydroxy-2-amino-4-methylsulphonyl-benzene
Conditions | Yield |
---|---|
Stage #1: 2-methoxy-5-(methylsulfonyl)aniline With boron tribromide In dichloromethane; chloroform at 0℃; for 0.333333h; Stage #2: With water; sodium hydrogencarbonate pH=7; | 15% |
With boron tribromide In dichloromethane for 5h; Reflux; | |
With boron tribromide |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
Conditions | Yield |
---|---|
With sodium hydroxide; nickel at 130℃; under 36775.4 Torr; Hydrogenation; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
tert-butylisonitrile
N-(tert-butyl)-2-(tert-butylimino)-6-(methylsulfonyl)-2H-benzo[b][1,4]oxazin-3-amine
Conditions | Yield |
---|---|
With palladium dichloride In 1,4-dioxane at 50℃; for 8h; | 89% |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
tert-butylisonitrile
N-(tert-butyl)-5-(methylsulfonyl)benzo[d]oxazol-2-amine
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane at 50℃; for 8h; | 88% |
Conditions | Yield |
---|---|
With acetic acid at 120℃; for 18h; | 80% |
Conditions | Yield |
---|---|
With N-methylcyclohexylamine; sulfur at 80℃; for 16h; Inert atmosphere; Sealed tube; | 80% |
Conditions | Yield |
---|---|
With sulfur; sodium sulfide pentahydrate; dimethyl sulfoxide at 70℃; for 16h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With N-methylcyclohexylamine; sulfur; dimethyl sulfoxide at 100℃; for 16h; Inert atmosphere; | 74% |
Conditions | Yield |
---|---|
With 4-methyl-morpholine; sulfur; dimethyl sulfoxide at 110℃; for 16h; Inert atmosphere; | 74% |
Conditions | Yield |
---|---|
With sulfur; acetic acid; dimethyl sulfoxide at 80℃; for 16h; Inert atmosphere; stereoselective reaction; | 72% |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
1-[trans-4-(ethyloxy)-1-methylcyclohexyl]-4-piperidinone
2-({1-[trans-4-(ethyloxy)-1-methylcyclohexyl]-4-piperidinyl}amino)-4-(methylsulfonyl)phenol
Conditions | Yield |
---|---|
Stage #1: 1-hydroxy-2-amino-4-methylsulphonyl-benzene; 1-[trans-4-(ethyloxy)-1-methylcyclohexyl]-4-piperidinone With polymer supported cyanoborohydride; acetic acid In tetrahydrofuran at 100℃; for 0.5h; Microwave; Stage #2: With ammonia In methanol; dichloromethane | 67% |
With acetic acid In dichloromethane at 100℃; Microwave irradiation; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
potassium ethyl xanthogenate
5-(methylsulfonyl)benzoxazole-2-thione
Conditions | Yield |
---|---|
With pyridine for 3h; Heating; | 57% |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
acrolein
5-(methylsulfonyl)quinolin-8-ol
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide In water for 2h; Skraup, Doebner-Miller Synthesis; Reflux; | 57% |
With hydrogenchloride In water at 100℃; for 1h; Skraup Quinoline Synthesis; Inert atmosphere; | 52% |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
1-[trans-1-methyl-4-(propyloxy)cyclohexyl]-4-piperidinone
2-({1-[trans-1-methyl-4-(propyloxy)cyclohexyl]-4-piperidinyl}amino)-4-(methylsulfonyl)phenol
Conditions | Yield |
---|---|
Stage #1: 1-hydroxy-2-amino-4-methylsulphonyl-benzene; 1-[trans-1-methyl-4-(propyloxy)cyclohexyl]-4-piperidinone With polymer supported cyanoborohydride; acetic acid In tetrahydrofuran at 100℃; for 1.5h; Microwave; Stage #2: With ammonia In methanol; dichloromethane | 35% |
With acetic acid In dichloromethane at 100℃; Microwave irradiation; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
2-Bromoacetyl bromide
6-(methylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In chloroform; water at 0 - 20℃; | 33% |
With caesium carbonate In N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
With polyphosphoric acid Heating; | 21% |
phosgene
1-hydroxy-2-amino-4-methylsulphonyl-benzene
5-methanesulfonyl-3H-benzooxazol-2-one
Conditions | Yield |
---|---|
With alkaline solution |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
2-amino-4-methanesulfonyl-6-nitrophenol
Conditions | Yield |
---|---|
With sulfuric acid; water; nitric acid |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
2-hydroxy-5-methanesulfonyl-benzenediazonium-betaine
1-hydroxy-2-amino-4-methylsulphonyl-benzene
4,4'-stilbenedicarbonyl dichloride
Conditions | Yield |
---|---|
Heating; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
1,4-naphthalenedicarboxylic acid dichloride
Naphthalene-1,4-dicarboxylic acid bis-[(2-hydroxy-5-methanesulfonyl-phenyl)-amide]
Conditions | Yield |
---|---|
Heating; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
2-Chloro-5-methanesulfonyl-benzooxazole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 57 percent / pyridine / 3 h / Heating 2: 100 percent / thionyl chloride, DMF / 0.5 h / 65 - 70 °C View Scheme |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
(5-Methanesulfonyl-benzooxazol-2-yl)-prop-2-ynyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 57 percent / pyridine / 3 h / Heating 2: 100 percent / thionyl chloride, DMF / 0.5 h / 65 - 70 °C 3: 21 percent / triethylamine / acetonitrile / 0.5 h / 65 - 70 °C View Scheme |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 57 percent / pyridine / 3 h / Heating 2: 100 percent / thionyl chloride, DMF / 0.5 h / 65 - 70 °C 3: 21 percent / triethylamine / acetonitrile / 0.5 h / 65 - 70 °C 4: silver tetrafluoroborate / CD3CN / 40 °C View Scheme |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: water / bei der Einwirkung von Sonnenlicht View Scheme |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: water / bei der Einwirkung von Sonnenlicht 3: aq. NaOH solution View Scheme |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
1-{trans-4-[(cyclopropylmethyl)oxy]-1-methylcyclohexyl}-4-piperidinone
2-[(1-{trans-1-methyl-4-[(cyclopropylmethyl)oxy]cyclohexyl}-4-piperidinyl)amino]-4-(methylsulfonyl)phenol
Conditions | Yield |
---|---|
With acetic acid In tetrahydrofuran at 100℃; for 1.5h; Microwave; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
1-{trans-1-methyl-4-[(1-methylethyl)oxy]cyclohexyl}-4-piperidinone
2-[(1-{trans-1-methyl-4-[(1-methylethyl)oxy]cyclohexyl}-4-piperidinyl)amino]-4-(methylsulfonyl)phenol
Conditions | Yield |
---|---|
With acetic acid In tetrahydrofuran at 100℃; for 1h; Microwave; |
1-hydroxy-2-amino-4-methylsulphonyl-benzene
naphthalene-2-carboxylate
5-(methylsulfonyl)-2-(naphthalen-2'-yl)benzo[d]oxazole
Conditions | Yield |
---|---|
With polyphosphoric acid at 110 - 120℃; for 16h; | 1.157 g |
Molecular Structure:
Molecular Formula: C7H9NO3S
Molecular Weight: 187.2163
IUPAC Name: 2-Amino-4-methylsulfonylphenol
Synonyms of Phenol,2-amino-4-(methylsulfonyl)- (CAS NO.98-30-6): 2-Amino-4-(methylsulfonyl)phenol ; CCRIS 5961 ; EINECS 202-654-4 ; 2-Amino-4-(methylsulphonyl)phenol
CAS NO: 98-30-6
Index of Refraction: 1.603
Molar Refractivity: 45.343 cm3
Molar Volume: 131.921 cm3
Surface Tension: 59.57 dyne/cm
Density: 1.419 g/cm3
Flash Point: 217.648 °C
Enthalpy of Vaporization: 71.942 kJ/mol
Boiling Point: 436.27 °C at 760 mmHg
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