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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393231Generated: October 30, 2026

HCID 22243789, compound → HCID 22649258, compound

https://huagongshe.com/reaction/393231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22243789HCID 22243789—
ReactantHCID 22649237HCID 22649237—
ProductHCID 22649258HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806274B1
Source datasetuspto-grants-2004_10
ORD IDord-e482d7a575f34d82805a5a2c1495c8c7
Source noteuspto-grants-2004_10