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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520138Generated: November 2, 2026

Quinoline, 1,2,3,4-tetrahydro-6-methoxy- → HCID 68194188, compound

https://huagongshe.com/reaction/1520138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoline, 1,2,3,4-tetrahydro-6-methoxy-HCID 67113—
ReactantMethyl 3-chloro-2-oxo-1,2-dihydroquinoxaline-6-carboxylateHCID 68194304—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 68194188HCID 6819418842%

Reaction Steps

To a solution of methyl 3-chloro-2-oxo-1,2-dihydroquinoxaline-6-carboxylate (700 mg, crude) in NMP (2 mL) was added 6-methoxy-1,2,3,4-tetrahydroquinoline (1.0 g, 6.13 mmol) with stifling for 3 h at 150° C. The reaction mixture was cooled to room temperature. The product was precipitated by the addition ethyl acetate and the solids were collected by filtration to afford methyl 3-(6-methoxy-1,2,3,4-tetrahydroquinolin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate as a light yellow solid (450 mg), which was used to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073902B2
Source datasetuspto-grants-2015_07
ORD IDord-65547aad8f0243ddbda9af6a5d6351ea
Source noteuspto-grants-2015_07