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2-aMino-6-nitrobenzaldehyde synthesis

6synthesis methods
98451-51-5 Synthesis
2-amino-6-nitrobenzyl alcohol

98451-51-5
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2-aMino-6-nitrobenzaldehyde

130133-53-8
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Yield:130133-53-8 88%

Reaction Conditions:

with manganese(IV) oxide in dichloromethane at 20; for 1 h;Inert atmosphere;

Steps:

115 6,7-Didehydro-17-methyl-5'-nitroquinolino[2',3':6,7]morphinan-3,14β-diol (29a)

5.1.115
6,7-Didehydro-17-methyl-5'-nitroquinolino[2',3':6,7]morphinan-3,14β-diol hydrochloride (SYK-350)
SYK-350 was prepared from compound 29a according to the procedure used to prepare SYK-27.
Yield, 87%; a light brown amorphous solid.
Mp 242-246 °C (dec). Anal. Calcd for C24H23N3O4·1.5HCl·0.8H2O: C, 59.24; H, 5.41; N, 8.64. Found: C, 59.35; H, 5.52; N, 8.48.

References:

Ida, Yoshihiro;Matsubara, Ayaka;Nemoto, Toru;Saito, Manabu;Hirayama, Shigeto;Fujii, Hideaki;Nagase, Hiroshi [Bioorganic and Medicinal Chemistry,2012,vol. 20,# 19,p. 5810 - 5831]