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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9303생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/9303

반응식

참여 물질

역할이름HCID투입량
반응물2-Tolyl isocyanateHCID 69194—
반응물tert-butyl N-[(4-aminophenyl)methyl]carbamateHCID 2756041—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 4-({[(2-methylphenyl)amino]carbonyl}amino)benzylcarbamateHCID 21032485—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091242B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-386fea515fe549098d963803cb3d34d0
출처 메모uspto-grants-2006_08