Reaktion #1741

ord-e14621919a904c08b3c9d56e77154681

Reaktionsgleichung

C[C@H]1[C@@H](O)O[C@@H]2OC3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3
dihydroqinghaosu
O=C=Nc1cccc([N+](=O)[O-])c1
m-nitrophenyl isocyanate
→
C[C@H]1[C@@H](O)O[C@@H]2OC3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3.O=C([O-])Nc1cccc([N+](=O)[O-])c1
title compound
C[C@H]1[C@@H](O)O[C@@H]2OC3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3.O=C([O-])Nc1cccc([N+](=O)[O-])c1
Dihydroqinghaosu M-Nitrobenzenecarbamate

Edukte

C[C@H]1[C@@H](O)O[C@@H]2OC3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3
dihydroqinghaosu
O=C=Nc1cccc([N+](=O)[O-])c1
m-nitrophenyl isocyanate

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was similarly prepared from dihydroqinghaosu and m-nitrophenyl isocyanate as Example 3.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726203uspto-grants-1998_03