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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917511Generated: November 1, 2026

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

https://huagongshe.com/reaction/917511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
Reactanttert-butyl N-[(4-aminophenyl)methyl]carbamateHCID 2756041—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-(4-{[(benzoylamino)carbothioyl]amino}benzyl)carbamateHCID 22000388100%

Reaction Steps

To a stirred solution of tert-butyl N-(4-aminobenzyl)carbamate (6.00 g, 27.0 mmol) in anhydrous THF (50 ml) was added benzoylisothiocyanate (4.43 g, 27.0 mmol). The solution was stirred for 2 hours and the solvent removed in vacuo to yield 100% (10.4 g) of the protected thiourea as a yellow solid: m.p. 161-163° C.; 1H-NMR (CDCl3) δ 1.45 (9H, s), 4.33 (2H, d), 4.85 (1H, broad), 7.34 (2H, d), 7.60 (5H, m), 7.90 (2H, d), 9.13 (1H, s), 12.58 (1H, s); 386 (ESMS, MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273880B2
Source datasetuspto-grants-2007_09
ORD IDord-6ecbaa8190654f7eac736c02a7a0deab
Source noteuspto-grants-2007_09