HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Isocyanato-1,2-dimethoxybenzene → N-(3,4-Dimethoxyphenyl)-N'-(1-methylpyrrolidin-2-ylidene)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Isocyanato-1,2-dimethoxybenzene | HCID 3517810 | — |
| Reactant | 1-Methyl-2-pyrrolidinimine | HCID 12448966 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(3,4-Dimethoxyphenyl)-N'-(1-methylpyrrolidin-2-ylidene)urea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998958 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-8669e24f341c46c7bc4bef0b3d89c539 |
| Source note | uspto-grants-1976_12 |