HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404548Generated: October 30, 2026
Cesium carbonate → 3-(5-(4-Cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yloxy)benzonitrile
https://huagongshe.com/reaction/404548
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Cyanophenol | HCID 13394 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (6-Chloro-pyridin-3-yl)-(4-cyclobutyl-[1,4]diazepan-1-yl)-methanone | HCID 58076653 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-(5-(4-Cyclobutyl-1,4-diazepane-1-carbonyl)pyridin-2-yloxy)benzonitrile | HCID 23624312 | — |
Reaction Steps
To a solution of (6-chloro-pyridin-3-yl)-(4-cyclobutyl-[1,4]diazepan-1-yl)-methanone (101.0 g, 343.8 mmol) in dimethylacetamide (1.1 L) was added Cs2CO3 (224 g, 687.6 mmol) and m-cyanophenol (81.9 g, 687.6 mmol). The resulting mixture was warmed to 125° C. and stirred for 20 h. After cooling to room temperature, the resulting mixture was filtered and acetic acid (1.5 L) was added to the filtrate. The resulting mixture was concentrated under reduced pressure to yield a brown residue which was taken up into MTBE (1.5 L) and 1N NaOH(aq) (1.5 L). The resulting layers were thoroughly mixed and then separated. The organic extract was dried over magnesium sulfate, filtered, and concentrated to yield the title compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748596B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-80205d6f699f418e953a6e26290db706 |
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| Source note | uspto-grants-2014_06 |
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