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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1829995Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1829995

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Tolyl isocyanateHCID 69194—
Edukttert-butyl N-[(4-aminophenyl)methyl]carbamateHCID 2756041—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-({[(2-methylphenyl)amino]carbonyl}amino)benzylcarbamateHCID 21032485—

Reaktionsschritte

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; Mine, 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07064229B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-280c85da84f0492bae20d2d6acbe1fec
Quellennotizuspto-grants-2006_06