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When heated with aniline and aniline hydrochloride they yield indulines.
The acid hydrochloride is the most valuable of all salts of quinine.
It is also prepared by heating trimethylamine hydrochloride.
They may also be obtained by the molecular rearrangement of the diazoamines, when these are warmed with the parent base and its hydrochloride.
Diazosuccinic ester, N2 C(C02C2H5)2, is similarly prepared by the action of nitrous acid on the hydrochloride of aspartic ester.