Hydrogen Bromide → HCID 13653512, compound
Reaction equation
[CH3:1][N:2]([N:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[C:19](=[O:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[F:26])[C:3](=[O:13])[CH2:4][NH:5]C(OC(C)(C)C)=O.[BrH:28]>CO>[BrH:28].[CH3:1][N:2]([N:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[C:19](=[O:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[F:26])[C:3](=[O:13])[CH2:4][NH2:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A slurry prepared from 1-[N-methyl-(t-butoxycarbonylamino)acetamido]-2-(2-fluorobenzoyl)pyrrole (20 g, 53.2 mmol) and 100 ml of methanol solution containing 12 ml of 48% HBr (0.106 mol) was stirred at room temperature for 6 hours. The resultant solution was evaporated to a solid which was recrystallized from isopropanol-ether to give 18 g (95%) of powder.
Workup
- customThe resultant solution was evaporated to a solid which
- customwas recrystallized from isopropanol-ether
Sources & evidence
- ORD record
- ord-5a18e76085664bf98c6d03ebecd7ce35
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04588727
Reaction notes
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