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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618445Generated: October 29, 2026

O-Toluidine → HCID 21850864, compound

https://huagongshe.com/reaction/618445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantHCID 21850843HCID 21850843—
SolventAcetonitrileHCID 6342—
ProductHCID 21850864HCID 2185086467%

Reaction Steps

Ethyl 4-methanesulfonyloxy-8-methoxy-1,7-naphthyridin-3-carboxylate (261 mg and o-toluidine (0.17 nl) were dissolved into 7 ml of acetonitrile and the solution was heated to reflex for 30 minutes. After cooling the mixture, the solvent was evaporated under reduced pressure and the beside was dissolved into chloroform. The solution was washed with water and then saturated sodium bicarbonate, dried, and concentrate under reduced pressure. The residue was subjected to silica gel column chromatography using a mixture of hexane:ethyl acetate (2:1) as an eluant to give yellow titled compound (180 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952504
Source datasetuspto-grants-1999_09
ORD IDord-07a148c089904c769dca0eab82d4d03c
Source noteuspto-grants-1999_09