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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168519Generated: November 1, 2026

Propargyl alcohol → 1H,7H-Pyrido[1,2,3-de]quinoxaline-6-carboxamide, N-[(4-chlorophenyl)methyl]-2,3-dihydro-9-(3-hydroxy-1-propynyl)-1-methyl-2,7-dioxo-

https://huagongshe.com/reaction/1168519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantN-(4-Chlorobenzyl)-9-iodo-1-methyl-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]-quinoxaline-6-carboxamideHCID 12083044—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
Product1H,7H-Pyrido[1,2,3-de]quinoxaline-6-carboxamide, N-[(4-chlorophenyl)methyl]-2,3-dihydro-9-(3-hydroxy-1-propynyl)-1-methyl-2,7-dioxo-HCID 10113864—

Reaction Steps

Propargyl alcohol (50 mg), cuprous iodide (50 mg) and a solution of PdCl2(PPh3)2 (1 mL, 0.15 M in THF) are added to a suspension of N-(4-chlorobenzyl)-9-iodo-1-methyl-2,7-dioxo-2,3-dihydro-1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamide (Preparation 23, 250 mg) in diethylamine (2.0 mL). The reaction is stirred for 90 min and the product is then extracted into chloroform and is chromatographed on silica gel. The desired product is eluted with 20% methanol/chloroform. Physical characteristics: 1H NMR (DMSO-d6) δ3.40, 4.36, 4.56, 5.22, 5.42, 7.36, 7.40, 7.44, 7.88, 8.76, 10.2. HRMS m/z 436.1064 (C23H18ClN3O4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624159B2
Source datasetuspto-grants-2003_09
ORD IDord-ec798d0535ed427381cf794d6c54af8a
Source noteuspto-grants-2003_09