HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-[{[di(2-chloroethyl)amino]carbonyl}amino]methanethioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Bis(2-chloroethyl)carbamoyl chloride | HCID 76346 | — |
| Reactant | 4-[(6,7-Dimethoxyquinolin-4-yl)oxy]aniline | HCID 11594543 | — |
| Reactant | [Di(2-chloroethyl)amino]methanoyl isothiocyanate | HCID 21890320 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [Di(2-chloroethyl)amino]methanoyl isothiocyanate | HCID 21890320 | — |
| Product | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-[{[di(2-chloroethyl)amino]carbonyl}amino]methanethioamide | HCID 21890592 | 55% |
Reaction Steps
[Di(2-chloroethyl)amino]methanoyl isothiocyanate was prepared using commercially available N,N-di(2-chloroethyl)carbamic chloride (80 mg) as a starting compound according to the description of the literature. [Di(2-chloroethyl)amino]methanoyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (48 mg, yield 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135466B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-16fca321b0cc4e8fa58a92e53dc66172 |
| Source note | uspto-grants-2006_11 |