Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 12083065 | HCID 12083065 | — |
| Product | HCID 10180536 | HCID 10180536 | 74% |
Reaction Steps
A dry flask is charged with N-(4-chlorobenzyl)-5-iodo-1-methyl-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]cinnoline-8-carboxamide (Preparation 40, 0.100 g), cuprous iodide (0.012 g), dichlorobistriphenylphosphine palladium (0.0072 g), propargyl alcohol (0.022 g), and diethylamine (4 mL). The reaction mixture is stirred at room temperature for 5 h and concentrated at reduced pressure. The residue is chromatographed, using 20 g of silica gel packed and eluted with EtOAc/CH2Cl2 (1/1), to obtain the title compound in 74% yield as a tan colored solid. Physical characteristics: M.p. 165-167° C.; 1H NMR (DMSO-d6) δ10.21, 8.67, 8.13, 7.74, 7.38, 5.41, 4.55, 4.35, 3.49, 3.12, 2.85; 13C NMR (DMSO-d6) δ173.69, 162.80, 144.92, 137.79, 133.56, 132.88, 130.54, 128.44, 127.97, 127.49, 126.10, 124.99, 117.98, 109.97, 90.12, 81.73, 48.60, 47.63, 43.24, 40.64, 17.64; MS (ESI+) m/z 422 (M+H)+; HRMS (FAB) m/z 422.1282 (C23H20ClN3O3+H); TLC (silica gel GF): Rf=0.22 acetone/chloroform (1/4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624159B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-ee7a02d391a445198465738d310d09ef |
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| Source note | uspto-grants-2003_09 |
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