HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyl-4-anisidine → (2-Chloro-6-nitroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyl-4-anisidine | HCID 22250 | — |
| Reactant | 2,4-Dichloro-6-nitroquinazoline | HCID 12703366 | — |
| Product | (2-Chloro-6-nitroquinazolin-4-yl)-(4-methoxyphenyl)-methylamine | HCID 11609884 | — |
Reaction Steps
The title compound was prepared from 2,4-dichloro-6-nitro-quinazoline and 4-methoxy-N-methylaniline by a procedure similar to example 10. 1H NMR (CDCl3): 8.31 (dd, J=9.6, 3.6, 1H), 7.78 (d, J=9.3, 1H), 7.73 (d, J=2.4, 1H), 7.21 (m, 2H), 7.06 (m, 2H), 3.90 (s, 3H), 3.69 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989462B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-2b6036b36a004006804a9fd7752fd82a |
| Source note | uspto-grants-2011_08 |