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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoyl isothiocyanateHCID 68284—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Dimethylaminomethylene-thioureidomethyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 7247466579.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265109B2
Source datasetuspto-grants-2007_09
ORD IDord-019b1077bec14d9b827da135577f82bf
Source noteuspto-grants-2007_09