HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914720Generated: October 30, 2026
Potassium Carbonate → 4-(3-Dimethylaminomethylene-thioureidomethyl)-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/914720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3-Dimethylaminomethylene-thioureidomethyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 72474665 | 79.2% |
Reaction Steps
A solution of 17.7 g (82.6 mmol) 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (commercially available) in 150 ml THF was treated with 11.1 ml (82.6 mmol) benzoyl isothiocyanate and stirred for 1 h at room temperature. After evaporation of the solvents the residue was taken up in 100 ml MeOH and treated with 34.2 g (248 mmol) potassium carbonate in 100 ml water. After stirring the mixture for 16 h at room temperature all volatiles were removed and the residue extracted with ethyl acetate. The combined organic layers were washed with saturated NaHCO3 solution and dried with MgSO4. After evaporation of the volatiles 88.1 ml (661 mmol) N,N-dimethylformamide dimethyl acetal was added and the mixture was heated to 110° C. for 16 h. The precipitate was filtered off, washed with n-hexane and dried to yield 21.5 g (79%) of the title compound as pink amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265109B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-019b1077bec14d9b827da135577f82bf |
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| Source note | uspto-grants-2007_09 |
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