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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168517Generated: October 25, 2026

Sodium hydride → Ethyl 9-iodo-1-methyl-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxylate

https://huagongshe.com/reaction/1168517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-amino-N-methylacetamideHCID 89675—
ReactantEthyl 2-(2,3-Difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoateHCID 69879816—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 9-iodo-1-methyl-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxylateHCID 1208304360.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Glycine methylamide (1.0 g) is added at room temperature to a solution of ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoate (Preparation 21, 2.0 g) in NMP (20 mL). Sodium hydride (400 mg, 60% dispersion in mineral oil) is added in two portions to the solution, and the solution is heated at 100° C. for 30 min. The product is partitioned between chloroform and water, the chloroform phase is concentrated and applied to a silica gel column with 1-2% methanol chloroform as the eluant. The purified fractions are triturated with ether to give 1.22 g of the title compound. Physical characteristics: M.p. 278-283° C.; 1H NMR (DMSO-d6) δ1.29, 3.63, 4.23, 5.10, 7.65, 8.09, 8.55. Anal. Found: C, 43.49; H, 3.18; N, 6.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624159B2
Source datasetuspto-grants-2003_09
ORD IDord-716885f811cd43c5882c170472049ab2
Source noteuspto-grants-2003_09