HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonate → 7-(N-benzylmorpholin-2-ylmethoxy)-4-(2-bromo-4-fluorophenoxy)-6-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | (4-Benzylmorpholin-2-yl)methanol | HCID 2776358 | — |
| Reactant | 4-(2-Bromo-4-fluorophenoxy)-7-hydroxy-6-methoxyquinazoline | HCID 135697906 | — |
| Product | 7-(N-benzylmorpholin-2-ylmethoxy)-4-(2-bromo-4-fluorophenoxy)-6-methoxyquinazoline | HCID 22243808 | — |
Reaction Steps
Using an analogous procedure to that described in the first paragraph of the portion of Note [140] immediately above which is concerned with the preparation of starting materials, the mesylate of N-benzylmorpholin-2-ylmethanol (Synth. Commun. 1980, 10, 59–73) was reacted with 4-(2-bromo-4-fluorophenoxy)-7-hydroxy-6-methoxyquinazoline (4.56 g) to give 7-(N-benzylmorpholin-2-ylmethoxy)-4-(2-bromo-4-fluorophenoxy)-6-methoxyquinazoline; Mass Spectrum: M+H+ 554 and 556.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001904B1 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-ba148dcc906a4eacb0b2e3606d0d4477 |
| Source note | uspto-grants-2006_02 |