Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Reactant | HCID 178522927 | HCID 178522927 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | HCID 491972 | HCID 491972 | 71% |
Reaction Steps
A solution of N-(4-chlorobenzyl)-4-hydroxy-8-iodo-6-(tetrahydro-2H-pyran-4-ylmethyl)-3-quinolinecarboxamide (0.16 g), PdCl2(PPh3)2, CuI (0.018 g) and 3-butyn-1-ol (0.03 mL) in 15 mL Et2NH is stirred at room temperature for 7 days. The solid in the reaction is filtered and rinsed with EtOAc. The filtrate is partitioned between EtOAc and H2O. The aqueous layer is extracted with EtOAc (3×). The organic layers and the solid previously filtered are combined, concentrated, adsorbed onto silica and chromatographed (gradient from CH2Cl2 to 4% MeOH in CH2Cl2). Product-containing fractions are combined and condensed to afford 101.6 mg (71%) of N-(4-chlorobenzyl)-2-(2-hydroxyethyl)-6-oxo-8-(tetrahydro-2H-pyran-4-ylmethyl)-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683181B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-d0a5427a349f432d86821072c7f1f785 |
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| Source note | uspto-grants-2004_01 |
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