HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichloro-2-isocyanatobenzene → 1-(2,6-Dichlorophenyl)-3-(6,7-dimethoxyquinazolin-4-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichloro-2-isocyanatobenzene | HCID 604537 | — |
| Reactant | 6,7-Dimethoxyquinazolin-4-amine | HCID 13060451 | — |
| Product | 1-(2,6-Dichlorophenyl)-3-(6,7-dimethoxyquinazolin-4-yl)urea | HCID 10271866 | — |
Reaction Steps
Using an analogous procedure to that described in Example 3, 2,6-dichlorophenyl isocyanate was reacted with 4-amino-6,7-dimethoxyquinazoline (European Patent Application No. 30156, Chemical Abstract volume 95, abstract 187290) to give the title compound; NMR Spectrum: (DMSOd6) 3.96 (s, 3H), 7.31 (m, 2H), 7.38 (t, 1H), 7.5 (d, 2H), 7.6 (d, 2H), 8.43 (s, 1H), 8.7 (s, 1H), 10.61 (s, 1H), 12.09 (s, 1H); Mass Spectrum M+H+ 393 & 395.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498335B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-a352f3faeaec4e41acb986fc86af8a56 |
| Source note | uspto-grants-2009_03 |