Hydrogen Bromide → HCID 53922314, compound

HRID 637637Notes

Reaction equation

HRID 637637 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

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-e9ee7cf3fea343c3a577c6105afebc4e
Source dataset
uspto-grants-1985_12
Patent number
US04558038

Reaction notes

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