Hydrogen Bromide → HCID 70584421, compound

HRID 1448727Notes

Reaction equation

HRID 1448727 reaction equation
[CH:1]1([NH:7][C:8](=[O:27])[C@H:9]([CH3:26])[NH:10][C:11](=[O:25])[C@H:12]([CH3:24])[NH:13]C(OCC2C=CC=CC=2)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[BrH:28]>C(O)(=O)C>[BrH:28].[CH:1]1([NH:7][C:8](=[O:27])[C@H:9]([CH3:26])[NH:10][C:11](=[O:25])[C@H:12]([CH3:24])[NH2:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 53997245HCID 53997245, compound

Product 1

HCID 70584421HCID 70584421, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

3.0 g of N-benzyloxycarbonyl-L-alanyl-L-alanine cyclohexylamide were treated with hydrogen bromide in acetic acid in a manner analogous to that described in Example 1(B)(ii) to give L-alanyl-L-alanine cyclohexylamide hydrobromide in the form of an oil.

Sources & evidence

ORD record
ord-f77fdffdc4574e229d9d4e4170d790ad
Source dataset
uspto-grants-1980_02
Patent number
US04187216

Reaction notes

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