HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-(chloromethyl)quinazoline → HCID 59242112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-(chloromethyl)quinazoline | HCID 13157520 | — |
| Reactant | N-Methyl-4-[(propan-2-yl)oxy]aniline | HCID 18002910 | — |
| Reactant | HCID 68518575 | HCID 68518575 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 59242112 | HCID 59242112 | — |
Reaction Steps
(2-Chloromethyl-quinazolin-4-yl)-(4-isopropoxy-phenyl)-methyl-amine: The title compound was prepared from 4-chloro-2-chloromethyl-quinazoline (300 mg, 1.4 mmol), 4-isopropoxy-N-methylaniline (279 mg, 1.7 mmol) and concd HCl (12 M, 10 drops) by a procedure similar to Example 203c with subsequent MPLC purification. 1H NMR (CDCl3) δ 7.8 (d, 1H), 7.55 (m, 1H), 7.10 (d, 2H), 7.0 (m, 2H), 6.9 (d, 2H), 4.7 (s, 2H), 4.5 (sept, 1H), 3.6 (s, 3H), 1.37 (d, 6H); LC-MS (ESI+; 342 ([M+H]+)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309562B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-a25f271e95d2467b89c1504ab2e54267 |
| Source note | uspto-grants-2012_11 |