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HRID 1829995作成日:2026年10月26日

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

https://huagongshe.com/reaction/1829995

反応式

関与物質

役割名称HCID仕込み量
反応物2-Tolyl isocyanateHCID 69194—
反応物tert-butyl N-[(4-aminophenyl)methyl]carbamateHCID 2756041—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-({[(2-methylphenyl)amino]carbonyl}amino)benzylcarbamateHCID 21032485—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07064229B2
出典データセットuspto-grants-2006_06
ORD IDord-280c85da84f0492bae20d2d6acbe1fec
出典メモuspto-grants-2006_06