HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238661Generated: October 31, 2026
1,1'-Thiocarbonyldiimidazole → tert-Butyl 4-carbamothioylpiperazine-1-carboxylate
https://huagongshe.com/reaction/238661
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-carbamothioylpiperazine-1-carboxylate | HCID 12093220 | 56.9% |
Reaction Steps
To a solution of thiocarbonyldiimidazole (2.1 g, 11.8 mmol) in tetrahydrofuran (30 mL) at room temperature, was added 1,1-dimethylethyl 1-piperazinecarboxylate (2 g, 10.75 mmol). The reaction mixture was stirred at room temperature for 2 h and then heated to 55° C. for additional 2 h. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure until approximately 20 mL of tetrahydrofuran remained. The residue was then treated with a 2 M solution of ammonia in methanol (10 mL) and stirred at room temperature for 24 h. The reaction mixture was concentrated under reduced pressure, and the residue was triturated with diethyl ether (25 mL) to give a white precipitate. The precipitate was filtered and dried to give 1.5 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642634B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-cda6c91cb0ba4bd4bdd248c7d4410322 |
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| Source note | uspto-grants-2014_02 |
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