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inquiryAppearance:white to yellow powder Storage:Inert atmosphere,Store in freezer, under -20°C Package:25kg/drum Application:Troglitazone is an an oral hypoglycemic agent which improves insulin sensitivity and decreases hepatic glucose production. Antidi
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inquiryTroglitazone CAS:97322-87-7 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 intermediat
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Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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TroglitazoneAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquiryTroglitazone
Conditions | Yield |
---|---|
With sodium tetrahydroborate; dimethylaminoacetic acid; sodium hydroxide In tetrahydrofuran; water at 20℃; | 84% |
With hydrogen; acetic acid In water; palladium |
5-[4-(6-benzyloxy-2,5,7,8-tetramethyl-chroman-2-ylmethoxy)-benzyl]-thiazolidine-2,4-dione
Troglitazone
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid at 70 - 80℃; debenzylation; | 70% |
thiourea
Ethyl 3-<4-<(6-acetoxy-2,5,7,8-tetramethylchroman-2-yl)methoxy>phenyl>-2-chloropropionate
A
Troglitazone
B
5-[4-(6-hydroxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]-2-iminothiazolidin-4-one
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h; Yield given. Multistep reaction. Yields of byproduct given; |
Troglitazone glucuronide
Troglitazone
Conditions | Yield |
---|---|
enzymatic treatment using glusulase; |
4-fluorobenzaldehyde
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium tert-butoxide / dimethylformamide / 8 h / 80 °C 2: AcOH; piperidine / toluene / 4 h / Heating 3: HCl / methanol / 0.25 h 4: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme |
trolox
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: imidazole / dimethylformamide 2: LAH / 3 h / 20 °C 3: potassium tert-butoxide / dimethylformamide / 8 h / 80 °C 4: AcOH; piperidine / toluene / 4 h / Heating 5: HCl / methanol / 0.25 h 6: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme | |
Multi-step reaction with 8 steps 1: toluene-4-sulfonic acid / 12 h / Reflux 2: dmap / dichloromethane / 2 h / 20 °C / Inert atmosphere 3: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 4: pyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere 5: potassium carbonate / N,N-dimethyl-formamide / 48 h / 2 °C / Inert atmosphere 6: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 7: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 8: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
(6-t-butyldimethylsilyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzo[1,2-b]pyran-2yl)methanol
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium tert-butoxide / dimethylformamide / 8 h / 80 °C 2: AcOH; piperidine / toluene / 4 h / Heating 3: HCl / methanol / 0.25 h 4: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme |
6-tert-butyl(dimethyl)silyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: LAH / 3 h / 20 °C 2: potassium tert-butoxide / dimethylformamide / 8 h / 80 °C 3: AcOH; piperidine / toluene / 4 h / Heating 4: HCl / methanol / 0.25 h 5: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme |
4-[6-(tert-butyl-dimethyl-silanyloxy)-2,5,7,8-tetramethyl-chroman-2-ylmethoxy]-benzaldehyde
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AcOH; piperidine / toluene / 4 h / Heating 2: HCl / methanol / 0.25 h 3: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme |
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HCl / methanol / 0.25 h 2: 84 percent / CoCl2; DMG; NaBH4 / NaOH / tetrahydrofuran; H2O / 20 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: t-BuOK / dimethylformamide / 1 h / 25 °C 1.2: 60 percent / dimethylformamide / 15 h / 25 °C 2.1: benzoic acid; piperidine / toluene / 4 h / 120 °C 3.1: 54 percent / Mg; MeOH / 8 h / 45 °C 4.1: 70 percent / HCl; AcOH / 70 - 80 °C View Scheme |
(6-Benzyloxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methanol
A
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: t-BuOK / dimethylformamide / 1 h / 25 °C 1.2: 60 percent / dimethylformamide / 15 h / 25 °C 2.1: benzoic acid; piperidine / toluene / 4 h / 120 °C 3.1: 54 percent / Mg; MeOH / 8 h / 45 °C 4.1: 70 percent / HCl; AcOH / 70 - 80 °C View Scheme |
4-[6-benzyloxy-2,5,7,8-tetramethylchroman-2-ylmethoxy]benzaldehyde
A
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: benzoic acid; piperidine / toluene / 4 h / 120 °C 2: 54 percent / Mg; MeOH / 8 h / 45 °C 3: 70 percent / HCl; AcOH / 70 - 80 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 54 percent / Mg; MeOH / 8 h / 45 °C 2: 70 percent / HCl; AcOH / 70 - 80 °C View Scheme |
2-hydroxymethyl-2,5,7,8-tetramethyl-chroman-6-ol
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1: 1.) NaH / 1.) DMF, rt, 1 h, 2.) benzene, rt, 1 h 2: 1.) NaH / 1.) DMSO, benzene, 60 deg C, 20 min, 2.) 60 deg C, 1 h 3: 94 percent / AcOH, 10percent H2SO4 / 0.17 h / 60 °C 4: 94 percent / pyridine / 1.) 10 deg C to rt, 2.) 30 deg C, 1 h 5: 98 percent / H2 / 10percent Pd-C / methanol; benzene / 3 h / 2325.2 - 2850.2 Torr 6: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 7: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
2-hydroxymethyl-6-methoxymethoxy-2,5,7,8-tetramethylchroman
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 1.) NaH / 1.) DMSO, benzene, 60 deg C, 20 min, 2.) 60 deg C, 1 h 2: 94 percent / AcOH, 10percent H2SO4 / 0.17 h / 60 °C 3: 94 percent / pyridine / 1.) 10 deg C to rt, 2.) 30 deg C, 1 h 4: 98 percent / H2 / 10percent Pd-C / methanol; benzene / 3 h / 2325.2 - 2850.2 Torr 5: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 6: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
6-Hydroxy-2,5,7,8-tetramethyl-2-<(4-nitrophenoxy)methyl>chroman
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 94 percent / pyridine / 1.) 10 deg C to rt, 2.) 30 deg C, 1 h 2: 98 percent / H2 / 10percent Pd-C / methanol; benzene / 3 h / 2325.2 - 2850.2 Torr 3: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 4: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
6-acetoxy-2-[(4-aminophenoxy)methyl]-2,5,7,8-tetramethylchromane
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 2: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
2,5,7,8-tetramethyl-6-acetoxy-2-(4-nitrophenyloxy)methylchroman
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 98 percent / H2 / 10percent Pd-C / methanol; benzene / 3 h / 2325.2 - 2850.2 Torr 2: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 3: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
6-(Methoxymethoxy)-2,5,7,8-tetramethyl-2-<(4-nitrophenoxy)methyl>chroman
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 94 percent / AcOH, 10percent H2SO4 / 0.17 h / 60 °C 2: 94 percent / pyridine / 1.) 10 deg C to rt, 2.) 30 deg C, 1 h 3: 98 percent / H2 / 10percent Pd-C / methanol; benzene / 3 h / 2325.2 - 2850.2 Torr 4: 1.) aq. NaNO2, conc. HCl, 2.) Cu2O / 1.) acetone, 0 deg C, 2.) 40 to 43 deg C, 30 min 5: 2.) AcOH, conc. HCl / 1.) sulfolane, 115 to 120 deg C, 80 min, 2.) H2O, 85 to 90 deg c, 12 h View Scheme |
(+/-)-5-<4-(6-hydroxy-2,5,7,8-tetramethyl-2H-chromen-2-ylmethoxy)benzyl>thiazolidine-2,4-dione
Troglitazone
Conditions | Yield |
---|---|
In methanol; palladium |
2-methoxy-ethanol
Ethyl 3-<4-<(6-acetoxy-2,5,7,8-tetramethylchroman-2-yl)methoxy>phenyl>-2-chloropropionate
Troglitazone
Conditions | Yield |
---|---|
With hydrogenchloride; thiourea In sulfolane |
carbonic acid tert-butyl ester 2-{4-[2,4-dioxo-thiazolidin-(5Z)-ylidenemethyl]phenoxymethyl}-2,5,7,8-tetramethyl-chroman-6-yl ester
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 2: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
carbonic acid tert-butyl ester 2-{4-[2,4-dioxothiazolidin-5-ylmethyl]phenoxymethyl}-2,5,7,8-tetramethylchroman-6-yl ester
Troglitazone
Conditions | Yield |
---|---|
With hydrogenchloride; water In acetonitrile for 0.75h; Reflux; |
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 2 °C / Inert atmosphere 2: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 3: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 4: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
6-tert-butoxycarbonyloxy-2,5,7,8-tetramethyl-chroman-2-carboxylic acid ethyl ester
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 2: pyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere 3: potassium carbonate / N,N-dimethyl-formamide / 48 h / 2 °C / Inert atmosphere 4: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 5: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 6: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
carbonic acid tert-butyl ester 2-hydroxymethyl-2,5,7,8-tetramethyl-chroman-6-yl ester
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: pyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere 2: potassium carbonate / N,N-dimethyl-formamide / 48 h / 2 °C / Inert atmosphere 3: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 4: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 5: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
carbonic acid tert-butyl ester 2-(4-formylphenoxymethyl)-2,5,7,8-tetramethyl-chroman-6-yl ester
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 2: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 3: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
ethyl 6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromene-2-carboxylate
Troglitazone
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1: dmap / dichloromethane / 2 h / 20 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere 3: pyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere 4: potassium carbonate / N,N-dimethyl-formamide / 48 h / 2 °C / Inert atmosphere 5: piperidine / ethanol / 12 h / Inert atmosphere; Reflux 6: palladium 10% on activated carbon; hydrogen / 1,4-dioxane / 20 h / 20 °C / 3620.13 Torr 7: hydrogenchloride; water / acetonitrile / 0.75 h / Reflux View Scheme |
Conditions | Yield |
---|---|
With pyridine for 48h; Ambient temperature; | 80% |
Troglitazone
5-[4-(2,5,7,8-tetramethyl-6-nicotinoyloxychroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione
Conditions | Yield |
---|---|
75% |
succinic acid anhydride
Troglitazone
Conditions | Yield |
---|---|
With dmap In dichloromethane for 48h; Reflux; | 63% |
With pyridine at 85℃; for 6h; | |
With pyridine In cyclohexane |
Troglitazone
5-[4-(6-benzoyloxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione
Conditions | Yield |
---|---|
62% |
Troglitazone
5-[4-(6-butyryloxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione
Conditions | Yield |
---|---|
56% |
Troglitazone
(2S,3S,4S,5R,6S)-3,4,5,6-Tetraacetoxy-tetrahydro-pyran-2-carboxylic acid methyl ester
methyl 2,3,4-tri-O-acetyl-1-O-<2-<4-<2,4-dioxothiazolidin-5-ylmethyl>phenoxymethyl>-2,5,7,8-tetramethylchroman-6-yl>-β-D-glucopyranuronate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In nitrobenzene at 85℃; under 20 Torr; for 4h; | 23% |
Troglitazone
Troglitazone glucuronide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 23 percent / p-toluenesulfonic acid monohydrate / nitrobenzene / 4 h / 85 °C / 20 Torr 2: 100 percent / 2.4percent aq.NaOH / methanol / 1 h / Ambient temperature View Scheme |
bromoacetic acid tert-butyl ester
Troglitazone
Di-t-butyl α,α'-{5-[4-(6-t-butoxycarbonylmethoxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl ]-2,4-dioxothiazolidine-3,5-diyl}diacetate
Conditions | Yield |
---|---|
With potassium carbonate In acetone |
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