Hydrochloric Acid → HCID 23064387, compound
Reaction equation
Cl.Cl.[CH3:3][O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[CH:11]=[N:10][CH:9]=[C:8]2[CH2:15]O.S(Cl)([Cl:19])=O>C(Cl)(Cl)Cl.C(OCC)C>[Cl:19][CH2:15][C:8]1[C:7]2[C:12](=[CH:13][CH:14]=[C:5]([O:4][CH3:3])[CH:6]=2)[CH:11]=[N:10][CH:9]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
The hydrochloride of the compound obtained in Step B (1.09 g; 0.005 mol) is suspended in 50 ml of chloroform. Thionyl chloride (2.80 ml; 0.04 mol) is added and then the reaction mixture is heated at reflux for 24 hours with stirring. After evaporation under reduced pressure, the residue obtained is taken up in ethyl ether. The precipitate formed is suction-filtered off and recrystallised from acetonitrile to yield the title compound in the form of a white solid.
Workup
- temperaturethe reaction mixture is heated
- temperatureat reflux for 24 hours
- customAfter evaporation under reduced pressure
- customthe residue obtained
- customThe precipitate formed
- filtrationis suction-filtered off
- customrecrystallised from acetonitrile
Sources & evidence
- ORD record
- ord-48b73efd8ba64b7c93e7d25f6e4d1490
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214689B2
Reaction notes
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