4,5-Dimethyl-1,3-dioxole-2-one
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) In tetrachloromethane at 85℃; for 16h; Inert atmosphere; | 95% |
With N-Bromosuccinimide In chloroform Reflux; Large scale; | 93.8% |
With N-Bromosuccinimide; dibenzoyl peroxide In tetrachloromethane at 77℃; for 6h; | 92% |
4,5-Dimethyl-1,3-dioxole-2-one
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With N-Bromosuccinimide In tetrachloromethane | 90% |
4-chloromethyl-5-methyl-1,3-dioxol-2-one
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With sodium bromide In N,N-dimethyl-formamide at 20℃; for 1h; | 75% |
With sodium bromide In N,N-dimethyl-formamide at 20℃; for 1h; | |
With sodium bromide In N,N-dimethyl-formamide at 20℃; for 1.5h; | |
With sodium bromide In N,N-dimethyl-formamide; acetone at 40 - 45℃; for 5h; Product distribution / selectivity; |
4,5-Dimethyl-1,3-dioxole-2-one
azobisisobutyronitrile
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With N-Bromosuccinimide In tetrachloromethane | 48% |
With N-Bromosuccinimide In tetrachloromethane |
N-Bromosuccinimide
4,5-Dimethyl-1,3-dioxole-2-one
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
2,2'-azobis(isobutyronitrile) In benzene at 20℃; for 0.5h; Heating / reflux; |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1H-imidazole-5-carboxylate
trityl olmesartan medoxomil
Conditions | Yield |
---|---|
Stage #1: 5-[4'-(bromomethyl)[1,1'-biphenyl]-2-yl]-2-(triphenylmethyl)-1H-tetrazole; ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1H-imidazole-5-carboxylate With tert-butylamine hydrobromide; potassium carbonate In acetone at 0 - 55℃; for 32h; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one With potassium carbonate; potassium iodide In acetone at 20 - 55℃; for 3h; | 98.5% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
ulifloxacin
prulifloxacin
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In N,N-dimethyl-formamide at 0℃; for 5h; Large scale; | 95.4% |
With potassium hydrogencarbonate In N,N-dimethyl-formamide for 5h; Ambient temperature; | 62% |
Stage #1: ulifloxacin With potassium hydrogencarbonate In acetonitrile at 25 - 30℃; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one at 15 - 30℃; for 27 - 28.25h; | |
Stage #1: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one; ulifloxacin With potassium hydrogencarbonate In N,N-dimethyl-formamide at 0 - 28℃; for 3 - 4h; Stage #2: With hydrogenchloride In chloroform; water for 0.25h; pH=0.8 - 1.0; | |
Stage #1: ulifloxacin With N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 0.166667h; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one In acetonitrile at 10 - 30℃; for 21h; Product distribution / selectivity; |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 95% |
carbon dioxide
L-phenylalanine
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide Ambient temperature; | 94% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl iodide
Conditions | Yield |
---|---|
With potassium iodide In acetone Ambient temperature; | 92% |
carbon dioxide
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
benzyl-methyl-amine
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide Ambient temperature; | 90% |
2-(6-(4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
C33H44ClN7O5SSi
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; | 89% |
6α,9α-difluoro-11β-hydroxy-16α,17α-isopropylidenedioxy-3-oxo-androsta-1,4-diene-17β-carbothioic acid
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate In water; ethyl acetate; N,N-dimethyl-formamide | 85% |
4-(1-methoxy-1-methylethyl)-2-propyl-1-{4-(2-trityltetrazol-5-yl)phenyl}phenylmethylimidazole-5-carboxylic acid
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
4-(1-methoxy-1-methylethyl)-2-propyl-1-{4-(2-trityltetrazol-5-yl)phenyl}phenylmethylimidazole-5-carboxylic acid-5-methyl-2-oxo-[1,3]-dioxolene-4-yl-methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide at 20℃; for 5h; | 84% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 6h; | 83% |
formic acid
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
4-formyloxymethyl-5-methyl-1,3-dioxolen-2-one
Conditions | Yield |
---|---|
With trimethylamine In acetonitrile at 20℃; for 1h; | 82% |
With triethylamine In acetonitrile for 1h; Ambient temperature; | 80% |
With triethylamine In acetonitrile for 2h; Ambient temperature; |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.333333h; Microwave irradiation; | 78% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
methyl 2-ethoxy-1-((2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl)methyl)-1H-benzo[d]-imidazole-7-carboxylate
Conditions | Yield |
---|---|
Stage #1: methyl 2-ethoxy-1-((2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl)methyl)-1H-benzo[d]-imidazole-7-carboxylate With potassium carbonate In N,N-dimethyl-formamide at -10 - 0℃; for 0.5h; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one In N,N-dimethyl-formamide at 20℃; | 77.5% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.416667h; Microwave irradiation; | 75% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 0.333333h; Microwave irradiation; | 74% |
Conditions | Yield |
---|---|
In toluene at 130℃; for 21h; Inert atmosphere; Schlenk technique; | 74% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
prulifloxacin
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 39.9℃; for 3h; | 72% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 24.9℃; Rate constant; also in presence of DIPA and TNBA, var concn. of DMDO-Br and amines; |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
(S)-3-(((tert-butoxycarbonyl)amino)methyl)-5-methylhexanoic acid
(S)-3-(tert-butoxycarbonylamino-methyl)-5-methyl-hexanoic acid 5-methyl-2-oxo-[1,3]dioxol-4-ylmethyl ester
Conditions | Yield |
---|---|
Stage #1: (S)-3-(((tert-butoxycarbonyl)amino)methyl)-5-methylhexanoic acid With caesium carbonate In methanol at 20℃; for 2h; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one In ISOPROPYLAMIDE | 72% |
Stage #1: (S)-3-(((tert-butoxycarbonyl)amino)methyl)-5-methylhexanoic acid With caesium carbonate In methanol at 20℃; for 2h; Stage #2: 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one In N,N-dimethyl acetamide | 72% |
carbon dioxide
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
benzylamine
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide Ambient temperature; | 70% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
N-benzyloxycarbonyl NFLX
N-benzyloxycarbonyl NFLX (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 60℃; | 69% |
4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In methanol; N,N-dimethyl-formamide | 68% |
tert-butyl 2-(methylamino)ethylcarbamate
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16h; | 67.4% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylate
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In N,N-dimethyl-formamide for 1h; Ambient temperature; | 66% |
With potassium hydrogencarbonate In N,N-dimethyl-formamide |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid
N-<(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl>norfloxacin
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In N,N-dimethyl-formamide for 5h; | 66% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid
N-<(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl>norfloxacin
Conditions | Yield |
---|---|
In N-methyl-acetamide; water | 66% |
4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one
S-(-)-6-fluoro-1-methyl-7-[4-(5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl-1-piperazinyl]-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at -5 - 5℃; for 3h; Product distribution / selectivity; | 63% |
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