HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748531Generated: October 30, 2026
Sodium hydride → HCID 178526264, compound
https://huagongshe.com/reaction/748531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12050204 | HCID 12050204 | — |
| Reactant | HCID 85873132 | HCID 85873132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178526264 | HCID 178526264 | 82.8% |
Reaction Steps
To a suspension of sodium hydride (0.05 g, 1.2 mmol, 60% dispersion in oil, pre-washed with hexane) in N,N-dimethylformamide (3 mL) was added a solution of 5-pyridin-3-yl-1,3-dihydro-2H-indol-2-one (0.19 g, 0.90 mmol) in N,N-dimethylformamide (4 mL). The mixture was stirred for 20 min under nitrogen atmosphere. 2-Chloro-5-(morpholin-4-ylmethyl)pyridine 1-oxide (0.14 g, 0.60 mmol), dissolved in N,N-dimethylformamide (3 mL) was added dropwise and the mixture was stirred at room temperature for 2 h and then heated at 130° C. for 1.5 h. The solvent was evaporated in vacuo and the residue was partitioned between 2 M HCl and ethyl acetate and the phases were separated. The aqueous layer was alkalized by addition of NaHCO3 (s) and extracted with ethyl acetate. The organic layer was dried (Na2SO4) and the solvent was removed in vacuo affording 200 mg of the title compound as a yellow solid: MS (ES) m/z 403 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399780B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-bf24637a24874f8993ce87b74853f523 |
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| Source note | uspto-grants-2008_07 |
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