HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518633Generated: October 30, 2026
Cesium carbonate → HCID 178472425, compound
https://huagongshe.com/reaction/518633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 178525752 | HCID 178525752 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178472425 | HCID 178472425 | 76% |
Reaction Steps
To a suspension of cis-4-(2-chloro-5-nitropyridin-4-ylamino)cyclohexanecarboxylic acid (5 g, 16.68 mmol) in toluene (111 mL) was added 2-(benzyloxy)ethanol (7.62 g, 50.0 mmol), cesium carbonate (16.31 g, 50.0 mmol), and 18-crown-6 (6.61 g, 25.02 mmol). The resulting mixture was purged with argon and stirred at 75° C. overnight. The mixture was allowed to cool to RT and diluted with EtOAc to about 150 mL total volume and washed sequentially with brine (2-150 mL), aqueous NH4Cl (2-150 mL) and water (150 mL). The organic phase was collected, dried over sodium sulfate and concentrated under reduced pressure. The residue was suspended in EtOH (111 mL) and thionyl chloride (36.5 mL, 500 mmol) was added dropwise via syringe. The reaction mixture was stirred at RT for 16 hours. The mixture was concentrated to ⅓ volume and diluted with DCM (150 mL). The organic portion was washed with aqueous NaHCO3 (100 mL), dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography (10-50% EtOAc/Hexanes) to afford cis-ethyl 4-(2-(2-(benzyloxy)ethoxy)-5-nitropyridin-4-ylamino)cyclohexanecarboxylate (5.6 g, 76% yield). MS m/z=444.2 [M+H]. Calc'd for C23H29N3O6: 443.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-515aad16511f4b0c88e936056505780b |
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| Source note | uspto-grants-2015_08 |
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