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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973921Generated: October 29, 2026

4-Isocyanato-1,2-dimethoxybenzene → N-(3,4-Dimethoxyphenyl)-N'-(1-methylpyrrolidin-2-ylidene)urea

https://huagongshe.com/reaction/1973921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isocyanato-1,2-dimethoxybenzeneHCID 3517810—
Reactant1-Methyl-2-pyrrolidinimineHCID 12448966—
SolventBenzeneHCID 241—
ProductN-(3,4-Dimethoxyphenyl)-N'-(1-methylpyrrolidin-2-ylidene)ureaHCID 54339111—

Reaction Steps

After dissolving 5.4 g. (0.055 mole) of 2 -imino-1 -methylpyrrolidine in dry benzene, 9.85 g. (0.055 mole) of 3,4 -dimethoxyphenylisocyanate (prepared according to the method of J. G. Lombardino and C. T. Gerber, J. Med. Chem., 7, Jan. 1964, p. 101 ), dissolved in dry benzene, is added dropwise to the solution. The reaction mixture is stirred at room temperature overnight (about 16 hrs.). The solvent is evaporated in vacuo and the residue, which solidifies on cooling, is triturated with anhydrous methanol. Repeated recrystallizations from methanol yields the pure product, 1 -(1 -methyl-2 -pyrrolidylidene)- 3 -(3,4 -dimethoxyphenyl)urea, m.p. = 118-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998958
Source datasetuspto-grants-1976_12
ORD IDord-8669e24f341c46c7bc4bef0b3d89c539
Source noteuspto-grants-1976_12