Boron tribromide → HCID 67277099, compound
Reaction equation
B(Br)(Br)Br.[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([O:31]CC2C=CC=CC=2)=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([S:18]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)(=[O:20])=[O:19])=[C:14]([C:27]([F:30])([F:29])[F:28])[CH:13]=2)[CH:11]=1>C(Cl)Cl>[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([OH:31])=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([S:18]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)(=[O:20])=[O:19])=[C:14]([C:27]([F:28])([F:29])[F:30])[CH:13]=2)[CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Boron tribromide (2.5 ml, 1.0 M in DCM) was added to a solution of the product from step b) (1.16 g) in DCM (15 ml) at 0° C. The solution was stirred for 15 min then quenched with water. The mixture was extracted with DCM (three times), the organic extracts were dried (MgSO4), evaporated and purified by chromatography (silica, petrol—ether as eluent) to give the sub-title compound (851 mg).
Workup
- customthen quenched with water
- extractionThe mixture was extracted with DCM (three times)
- dry with materialthe organic extracts were dried (MgSO4)
- customevaporated
- custompurified by chromatography (silica, petrol—ether as eluent)
Sources & evidence
- ORD record
- ord-42a1ced72c844f87add3d2f68ec4439a
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163727B2
Reaction notes
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