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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223064Generated: October 31, 2026

4-Methoxy-2-methylphenyl isocyanate → N-(7-chloro-2,3-dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-N'-(4-methoxy-2-methylphenyl)-urea

https://huagongshe.com/reaction/2223064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-methylphenyl isocyanateHCID 2734905—
Reactant3-amino-7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-oneHCID 22135266—
SolventDichloromethaneHCID 6344—
ProductN-(7-chloro-2,3-dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-N'-(4-methoxy-2-methylphenyl)-ureaHCID 10151750—

Reaction Steps

To a solution of 3-amino-7-chloro-5-phenyl-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one (INTERMEDIATE 1) (0.299 g, 1 mmol) in dichloromethane (15 ml) was added 1-isocyanato-4-methoxy-2-methyl-benzene (0.163 g, 1 mmol). The reaction mixture was stirred at room temperature for 17 hours. The solvent was evaporated in vacuo, the residue was triturated with ether and the title compound was obtained as a colorless solid (0.197 g, 42%). 1H-NMR (CDCl3): δ 7.57-7.48 (m, 3H), 7.47-7.44 (m, 1H), 7.39-7.38 (m, 3H), 7.36-7.29 (m, 2H), 6.77-6.73 (m, 2H), 6.71 (d, J=2.8 Hz, 1H), 6.61 (s, 1H), 5.51 (d, J=8.4 Hz, 1H), 3.78 (s, 3H), 3.39 (s, 3H) and 2.29 (s, 3H). MS (ESI) (M+H)+=463.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375101B2
Source datasetuspto-grants-2008_05
ORD IDord-2cd7c575798e464190ab7f0e56a06a86
Source noteuspto-grants-2008_05