Sodium Azide → HCID 11037520, compound
Reaction equation
[Br:1]N1C(=O)CCC1=O.[C:9]([O:17][CH2:18][CH2:19][O:20][CH2:21][N:22]1[CH:29]=[C:28]([CH:30]=[CH2:31])[C:26](=[O:27])[NH:25][C:23]1=[O:24])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[N-:32]=[N+:33]=[N-:34].[Na+]>COCCOC.O>[C:9]([O:17][CH2:18][CH2:19][O:20][CH2:21][N:22]1[CH:29]=[C:28]([CH:30]([N:32]=[N+:33]=[N-:34])[CH2:31][Br:1])[C:26](=[O:27])[NH:25][C:23]1=[O:24])(=[O:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
N-Bromosuccinimide (NBS, 350 mg, 1.96 mmol) was added in aliquots to a precooled (−5° C.) suspension prepared by mixing a solution of 3 (61 mg, 1.95 mmol) in 1,2-dimethoxyethane (25 ml) with a solution of sodium azide (510 mg, 7.84 mmol) in water (1.2 ml). The initial yellow color faded away after each addition. When all the NBS was consumed, the reaction mixture was allowed to stand at 0° C. for 30 min., prior to pouring onto ice-water (25 ml), and extraction with dichloromethane (3×50 ml). The dichloromethane extract was washed with cold water (25 ml), dried (Na2SO4), the solvent was removed in vacuo to yield a residue which was purified by elution from a silica gel column using chloroform:methanol (98:2, v/v) as eluent to yield 4 (388 mg, 45.5%) as a viscous oil which was used in the next reaction.
Workup
- customprepared
- additionafter each addition
- customWhen all the NBS was consumed
- additionto pouring onto ice-water (25 ml), and extraction with dichloromethane (3×50 ml)
- extractionThe dichloromethane extract
- washwas washed with cold water (25 ml)
- dry with materialdried (Na2SO4)
- customthe solvent was removed in vacuo
- customto yield a residue which
- customwas purified by elution from a silica gel column
Sources & evidence
- ORD record
- ord-210fe1a089494fb2bce0f33c50ee0d99
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07589077B2
Reaction notes
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