HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22243789, compound → HCID 22649258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22243789 | HCID 22243789 | — |
| Reactant | HCID 22649237 | HCID 22649237 | — |
| Product | HCID 22649258 | HCID 22649258 | — |
Reaction Steps
Using an analogous procedure to that described in the second last paragraph of Note [115] above, 6-(2-methylimidazol-1-yl)-1-hexyne was reacted with 4-(2-bromo-4-fluorophenoxy)-6-methoxy-7-trifluoromethanesulphonyloxyquinazoline to give 4-(2-bromo-4-fluorophenoxy)-6-methoxy-7-[6-(2-methylimidazol-1-yl)-1-hexynyl]quinazoline; NMR Spectrum: (DMSOd6) 1.56 (m, 2H), 1.85 (m, 2H), 2.28 (s, 3H), 2.56 (m, 2H), 3.9 (m, 2H), 3.98 (s, 3H), 6.75 (br m, 1H), 7.1 (br m, 1H), 7.36-7.82 (m, 3H), 7.63 (s, 1H), 7.98 (s, 1H), 8.61 (s, 1H); Mass Spectrum: M+H+ 509 and 511.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806274B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-e482d7a575f34d82805a5a2c1495c8c7 |
| Source note | uspto-grants-2004_10 |