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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976124Generated: October 30, 2026

Benzoyl isothiocyanate → tert-butyl N-[(4-{[(benzoylamino)carbothioyl]amino}cyclo-hexyl)methyl]carbamate

https://huagongshe.com/reaction/1976124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant1,1-Dimethylethyl N-((4-aminocyclohexyl)methyl)carbamateHCID 21882540—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-[(4-{[(benzoylamino)carbothioyl]amino}cyclo-hexyl)methyl]carbamateHCID 1552426591.2%

Reaction Steps

A solution of tert-butyl N-[(4-aminocyclohexyl)methyl]carbamate (4.683 g, 20.5 mmol) and benzoyl isothiocyanate (3.77 g, 23.1 mmol) in 180 ml THF was stirred at room temperature for 20 hours. The solvent was removed in vacuo to yield a golden viscous oil. The oil was triturated with 250 ml hexane and the resulting solid was collected by filtration and washed with hexane. The off-white solid was washed several times with hexane and was dried under vacuum to yield 91% (7.32 g) of the desired product as an off-white solid: 1H-NMR (CDCl3) δ 1.20 (6H, m), 1.44 (9H, s), 1.83 (2H, m), 2.25 (2H, m), 3.01 (2H, t, J=6.4 Hz), 4.20 (1H, m), 4.62 (1H, m), 7.51 (2H, t, J=7.9 Hz), 7.60 (1H, t, J=7.4 Hz), 7.81 (2H, d, J=7.2 Hz), 8.93 (1H, s); 392 (ESMS, MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225330B1
Source datasetuspto-grants-2001_05
ORD IDord-f50796cb7f764038865d7fa733d0d4ca
Source noteuspto-grants-2001_05