Ethanol → HCID 69198568, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([C:11]2[CH:16]=[C:15]([C:17]3[O:21][C:20]([P:22]([OH:25])([OH:24])=[O:23])=[C:19]([CH2:26][CH3:27])[C:18]=3[CH2:28][CH3:29])[CH:14]=[C:13]([C:30]([OH:32])=[O:31])[CH:12]=2)=[O:10])[CH:5]=[CH:6][CH:7]=1.[CH3:33][CH2:34]N=C=NCCCN(C)C.C(O)C>CN(C1C=CN=CC=1)C.C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([C:11]2[CH:16]=[C:15]([C:17]3[O:21][C:20]([P:22]([OH:25])([OH:24])=[O:23])=[C:19]([CH2:26][CH3:27])[C:18]=3[CH2:28][CH3:29])[CH:14]=[C:13]([C:30]([O:32][CH2:33][CH3:34])=[O:31])[CH:12]=2)=[O:10])[CH:5]=[CH:6][CH:7]=1Participants
6
Procedure
A mixture of 1-(3-bromophenylcarbamoyl)-3-carboxy-5-(diethyl 2-phosphonofuran-5-yl)benzene (1 mmol), EDCI (2 mmol), DMAP (0.1 mmol) and ethanol (1.5 mmol) in 70 mL of CH2Cl2 were stirred at rt for 14 h. After evaporation the mixture was redissolved in MeOH and slurried with 5 g of DOWEX 50WX8-400 free acid and 5 g of DOWEX 1X8-400 bicarbonate resin for 4 h and then filtered. The filtrate was evaporated to provide 1-(3-bromophenylcarbamoyl)-3-carboethoxy-5-(diethyl 2-phosphonofuran-5-yl)benzene.
Workup
- customAfter evaporation the mixture
- dissolutionwas redissolved in MeOH
- waitslurried with 5 g of DOWEX 50WX8-400 free acid and 5 g of DOWEX 1X8-400 bicarbonate resin for 4 h
- filtrationfiltered
- customThe filtrate was evaporated
Sources & evidence
- ORD record
- ord-9b2e3b9af8d34ab4be3f7763e04ad656
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06919322B2
Reaction notes
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