HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459802Generated: October 29, 2026
Benzylamine → 4-(3-Benzylamino-2-cyano-6-fluoro-phenyl)-piperazine-1-carboxylic Acid Tert-butyl Ester
https://huagongshe.com/reaction/459802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58901904 | HCID 58901904 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Benzylamino-2-cyano-6-fluoro-phenyl)-piperazine-1-carboxylic Acid Tert-butyl Ester | HCID 58824126 | — |
Reaction Steps
To 655 mg (2.03 mmol) of 4-(2-cyano-3,6-difluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester dissolved in 10 mL DMF was added 560 mg (2 eq., 4.06 mmol) potassium carbonate and 243 μL (1.1 eq., 2.22 mmol) benzylamine. The mixture was heated to 100° C. for 5 days, cooled to room temperature and partitioned between ethyl acetate and water, dried over magnesium sulfate and concentrated. 4-(3-Benzylamino-2-cyano-6-fluoro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (288 mg) was precipitated from dichloromethane/hexanes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196087B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-4cf98c1a8fae4c5a9287a973f2e85ef1 |
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| Source note | uspto-grants-2007_03 |
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