HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853213Generated: October 29, 2026
Water → 7-Benzyloxy-6-cyano-4-(3-fluoro-4-nitrophenoxy)quinoline
https://huagongshe.com/reaction/853213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Fluoro-4-nitrophenol | HCID 520948 | — |
| Reactant | 7-Benzyloxy-4-chloro-6-cyanoquinoline | HCID 22646519 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 7-Benzyloxy-6-cyano-4-(3-fluoro-4-nitrophenoxy)quinoline | HCID 22936649 | 40% |
Reaction Steps
The 7-benzyloxy-4-chloro-6-cyanoquinoline (8.82 g, 30.0 mmol) described in WO98/13350 was suspended in 1-methylpyrrolidone (30 ml), and then 3-fluoro-4-nitrophenol (5.18 g, 33.0 mmol) and N,N-diisopropylethylamine (3.88 g, 30.0 mmol) were added and the mixture was heated and stirred at 110° C. for 4 hours. After returning the reaction system to room temperature, water was added and a solid precipitated. The obtained solid was filtered out, washed with water, methanol and ethyl acetate and dried at 60° C. to obtain the title compound (4.98 g, 12.0 mmol, 40%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253286B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-40c2904126a74f718b043315e7309fda |
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| Source note | uspto-grants-2007_08 |
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