HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252870Generated: October 30, 2026
Dichloromethane → 4-(4-Cyanobenzyl)piperazine-1-carbothioamide
https://huagongshe.com/reaction/252870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Reactant | 1-Boc-4-(4-Cyanobenzyl)piperazine | HCID 18382257 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(4-Cyanobenzyl)piperazine-1-carbothioamide | HCID 86040437 | 50% |
Reaction Steps
A solution of tert-butyl 4-(4-cyanobenzyl)piperazine-1-carboxylate (336, 1.374 g, 4.56 mmol) in DCM (5 mL) and TFA (5 mL) was stirred at room temperature for one hour. The reaction mixture was concentrated and the residue was added to a solution of thiocarbonyldiimidazole (1.21 g, 6.84 mmol, 1.5 equiv.) in dry DCM (20 mL) under N2 at 0° C. Obtained solid was diluted with MeOH (20 mL) and transferred to a pressure vial. Ammonia gas was bubbled in for 10 min and the flask was capped and stirred at 80° C. for two days. The reaction mixture was concentrated and purified by flash chromatography using 60% EtOAc in hexane as an eluent, to afford the title compound 337 (593 mg, 50% yield). MS: calc: 260.1; found: 261.2 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868205B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-903b24d46f9d4024862180afb5f5ca09 |
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| Source note | uspto-grants-2011_01 |
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