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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255859Generated: October 26, 2026

2-Amino-5-methylbenzoic acid → HCID 13959036, compound

https://huagongshe.com/reaction/255859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylbenzoic acidHCID 76255—
Reactant2-Amino-3-methylbenzoic acidHCID 78101—
ReactantMethyl 2-Amino-5-methylbenzoateHCID 1201104—
Reactant2-(2-Amino-5-methyl-phenyl)-propan-2-olHCID 13959001—
Reactant2-(2-Amino-5-methylphenyl)propeneHCID 13959003—
Reactant4,6-DimethylcinnolineHCID 13959005—
Reactant6-Methyl-4-(trichloromethyl)cinnolineHCID 13959007—
ProductHCID 13959036HCID 13959036—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699651
Source datasetuspto-grants-1987_10
ORD IDord-064095af81d340538ef50470603e61ca
Source noteuspto-grants-1987_10