Reaktion #343041

ord-064095af81d340538ef50470603e61ca

Reaktionsgleichung

Cc1ccc(N)c(C(=O)O)c1
2-amino-5-methylbenzoic acid
C=C(C)c1cc(C)ccc1N
2-(2-amino-5-methylphenyl)propene
COC(=O)c1cc(C)ccc1N
methyl 2-amino-5-methylbenzoate
Cc1ccc(N)c(C(C)(C)O)c1
(2-amino-5-methylphenyl)dimethylcarbinol
Cc1ccc2nncc(C)c2c1
4,6-dimethylcinnoline
Cc1ccc2nncc(C(Cl)(Cl)Cl)c2c1
6-methyl-4-(trichloromethyl)cinnoline
Cc1cccc(C(=O)O)c1N
2-amino-3-methylbenzoic acid
Cc1ccc2nncc(C(=O)O)c2c1
6-Methylcinnoline-4-carboxylic acid

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

51 was prepared, as a tan solid, m.p.: 179°-180° C., from 2-amino-5-methylbenzoic acid, by the respective procedures described in Example 49 for preparing 49 from 2-amino-3-methylbenzoic acid: via methyl 2-amino-5-methylbenzoate (a solid, m.p.: 62°-63° C.), (2-amino-5-methylphenyl)dimethylcarbinol (an oil, b.p.: 100° C./0.1 Torr.), 2-(2-amino-5-methylphenyl)propene (a liquid, b.p.: 87°-90° C./0.5 Torr.), 4,6-dimethylcinnoline (a solid, m.p.: 75°-76° C.), and 6-methyl-4-(trichloromethyl)cinnoline (green crystals, m.p.: 132°-133° C., with decomposition).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04699651uspto-grants-1987_10