HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390708Generated: October 25, 2026
Cesium carbonate → (NZ)-N-(5-methyl-3-phenyl-1,3-thiazol-2-ylidene)pyrrolidine-1-carboxamide
https://huagongshe.com/reaction/390708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | 5-Chloro-1,10-phenanthroline | HCID 77865 | — |
| Reactant | N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide | HCID 47197229 | — |
| Reactant | Water ammonium hydroxide | HCID 86589665 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (NZ)-N-(5-methyl-3-phenyl-1,3-thiazol-2-ylidene)pyrrolidine-1-carboxamide | HCID 87449702 | — |
Reaction Steps
To a 4 mL vial equipped with a septum cap and stir bar was added N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide (21 mg, 0.1 mmol), copper(I) trifluoromethanesulfonate benzene complex (10 mg, 0.02 mmol), 5-chloro-1,10-phenanthroline (8.5 mg, 0.04 mmol) and cesium carbonate (38.9 mg, 0.12 mmol). The mixture was placed under a nitrogen atmosphere. Iodobenzene (0.12 mmol) in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the mixture. The reaction mixture was heated at 120° C. for overnight. A solution of concentrated ammonium hydroxide/water (1:2, 1 mL) was added and the mixture was filtered and solvent removed under reduced pressure. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383657B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-b9a1c7ad96754a8e8302465963d697d4 |
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| Source note | uspto-grants-2013_02 |
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