HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391288Generated: October 26, 2026
Ethanesulfonamide → N-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide
https://huagongshe.com/reaction/391288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanesulfonamide | HCID 73702 | — |
| Reactant | 2-Chloro-4-(5-formyl-pyridin-3-yl)-benzonitrile | HCID 59578397 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide | HCID 49819978 | — |
Reaction Steps
Titanium(IV) isopropoxide (0.365 mL, 1.245 mmol) was added to a mixture of 2-chloro-4-(5-formylpyridin-3-yl)benzonitrile (as prepared in Example 23, step 1; 0.151 g, 0.622 mmol), ethanesulfonamide (0.085 g, 0.778 mmol) in toluene (10 mL) at room temperature. The resulting mixture was heated to reflux for 4 h. After concentration, the residue was dissolved in THF (5 mL), and cooled to −40° C. Cyclopropylmagnesium bromide (3.73 mL, 1.867 mmol) was added dropwise, and the resulting mixture was slowly warmed up to room temperature and stirred overnight. After quenching by saturated NH4Cl solution, the residue was purified by flash column (ethyl acetate-heptane, v/v, 40%-60%) yielded a slightly yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383827B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-19c0ac6ff92446fdb5ca8e05b366bbd4 |
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| Source note | uspto-grants-2013_02 |
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