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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9303Generated: October 25, 2026

2-Tolyl isocyanate → Tert-butyl 4-({[(2-methylphenyl)amino]carbonyl}amino)benzylcarbamate

https://huagongshe.com/reaction/9303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tolyl isocyanateHCID 69194—
Reactanttert-butyl N-[(4-aminophenyl)methyl]carbamateHCID 2756041—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-({[(2-methylphenyl)amino]carbonyl}amino)benzylcarbamateHCID 21032485—

Reaction Steps

2-Methylphenylisocyanate (7.57 g, 59.83 mmol) was added dropwise at 0° C. to a solution of (4-amino-benzyl)-carbamic acid tert-butyl ester (13.30 g, 59.83 mmol, prepared analoguous to: Moloney, Gerard P.; Martin, Graeme R.; Mathews, Neil; Milne, Aynsley; Hobbs, Heather; et al. J Med. Chem. 1999, 42, 2504–2526) in 120 mL DCM. The reaction was heated under reflux for 16 h, cooled to r.t. and the precipitated product was collected by filtration and dried in vacuum (19.20 g, 54.00 mmol). M.p. 200–202° C.; TLC (PE/EtOAc 1/1) Rf 0.65; 1H NMR (400 MHz, D6-DMSO) δ 1.39 (s, 9H); 2.24 (s, 3H); 4.06 (d, J=6 Hz, 2H); 6.93 (mc, 1H); 7.12–7.17 (m, 4); 7.32 (mc, 1H); 7.40 (mc, 2H); 7.85 (mc, 1H); 7.90 (s, 1H); 8.98 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091242B2
Source datasetuspto-grants-2006_08
ORD IDord-386fea515fe549098d963803cb3d34d0
Source noteuspto-grants-2006_08