Hydrogen Bromide → HCID 53922314, compound
Reaction equation
C([NH:11][C@H:12]([C:14]([N:16]([C:21]1[CH:25]=[CH:24][S:23][CH:22]=1)[CH2:17][C:18]([OH:20])=[O:19])=[O:15])[CH3:13])(OCC1C=CC=CC=1)=O.Br>C(O)(=O)C>[NH2:11][C@H:12]([C:14]([N:16]([C:21]1[CH:25]=[CH:24][S:23][CH:22]=1)[CH2:17][C:18]([OH:20])=[O:19])=[O:15])[CH3:13]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner described in example 5B, N-carbobenzyloxy-L-alanyl-N-(3-thienyl)glycine was treated with anhydrous hydrogen bromide in acetic acid to yield the hydrobromide salt of L-alanyl-N-(3-thienyl)glycine.
Sources & evidence
- ORD record
- ord-769d0f9be7764f269680db86100ee741
- Source dataset
- uspto-grants-1985_01
- Patent number
- US04496542
Reaction notes
Loading…