(1-methyl-5-nitro-1H-imidazol-2-yl)methyl 4-nitrophenyl carbonate
ronidazole
Conditions | Yield |
---|---|
With ammonium hydroxide In dichloromethane at 0 - 10℃; for 3h; Inert atmosphere; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 20 °C / Inert atmosphere 2: ammonium hydroxide / dichloromethane / 3 h / 0 - 10 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 94% |
Conditions | Yield |
---|---|
In ethanol; acetone for 24h; Reflux; | 89% |
potassium tetrachloroplatinate(II)
ronidazole
(NO2CCHNC(CH2OC(O)NH2)N(CH3))2PtCl2
Conditions | Yield |
---|---|
In water solid ligand added to aq. soln. of K2(PtCl4), stirred at 50 °C for 1 h; ppt. filtered, washed with EtOH/Et2O, Et2O, dried in vac.; elem. anal.; | 81% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 81% |
Conditions | Yield |
---|---|
In ethanol; acetone for 4h; Reflux; | 78.86% |
Conditions | Yield |
---|---|
In ethanol; acetone for 24h; Reflux; | 78.67% |
Conditions | Yield |
---|---|
In ethanol; acetone for 4h; Reflux; | 76.86% |
Conditions | Yield |
---|---|
In ethanol; dichloromethane; acetone for 4h; Reflux; | 74.96% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 73% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 73% |
Conditions | Yield |
---|---|
In ethanol; acetone for 24h; Reflux; | 69% |
Conditions | Yield |
---|---|
In ethanol; acetone for 4h; Reflux; | 68.04% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 62% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 60% |
Conditions | Yield |
---|---|
With ammonia; potassium carbonate In methanol at 50℃; for 18h; | 59% |
Conditions | Yield |
---|---|
In ethanol; acetone for 4h; Reflux; | 58.71% |
Conditions | Yield |
---|---|
In ethanol; acetone for 2.5h; Reflux; | 58% |
Conditions | Yield |
---|---|
With sodium hydroxide; NaH2PO4 buffer at 37℃; for 120h; | 36 % Chromat. |
Conditions | Yield |
---|---|
at 20 - 100℃; for 18h; Inert atmosphere; |
ronidazole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 18 h / 20 - 100 °C / Inert atmosphere 2: triethylamine; thionyl chloride / dichloromethane / 0 °C / Reflux; Inert atmosphere 3: dichloromethane; acetonitrile / 20 - 60 °C / Inert atmosphere View Scheme |
ronidazole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 18 h / 20 - 100 °C / Inert atmosphere 2: triethylamine; thionyl chloride / dichloromethane / 0 °C / Reflux; Inert atmosphere 3: dichloromethane; acetonitrile / 20 - 60 °C / Inert atmosphere View Scheme |
ronidazole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 18 h / 20 - 100 °C / Inert atmosphere 2: triethylamine; thionyl chloride / dichloromethane / 0 °C / Reflux; Inert atmosphere View Scheme |
1. | mmo-sat 3 µg/plate | CBINA8 Chemico-Biological Interactions. 49 (1984),27. | ||
2. | mmo-smc 500 ppm | MUREAV Mutation Research. 86 (1981),243. | ||
3. | orl-rat LD50:3400 mg/kg | VMDNAV Veterinarno-Meditsinski Nauki. 22 (7)(1985),90. | ||
4. | ipr-rat LD50:1500 mg/kg | VMDNAV Veterinarno-Meditsinski Nauki. 22 (7)(1985),90. |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View