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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936780Generated: October 29, 2026

(6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amine → HCID 22609780, compound

https://huagongshe.com/reaction/1936780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amineHCID 1569266—
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22609780HCID 2260978060%

Reaction Steps

The (4-benzyloxy-phenyl)-(6-bromoquinazolin-4-yl)-amine (200 mg, 0.49 mmol), 2-(tributylstannyl)thiophene (200 mg, 0.53 mmol) and bis(triphenylphosphine)palladium(II) chloride (catalytic) were dissolved in dioxan (3 ml) and heated at reflux under nitrogen for 4 hr. The cooled reaction mixture was absorbed onto silica and purified by flash column chromatography (silica gel, eluting with an ethyl acetate/iso-hexane gradient). The resulting solid was triturated with iso-hexane/ethyl acetate to give the product (120 mg, 60%) as a pale yellow solid; δH [2H6]-DMSO 9.88 (1H, b, NH), 8.76 (1H, s, 5-H), 8.49 (1H, s, 2-H), 8.12 (1H, d, 7-H), 7.82-7.60 (5 H, m, thiophene-3-H, thiophene-5-H, 8-H, 2′-H, 6′-H), 7.52-7.30 (5H, m, 5×Ph-H), 7.23 (1H, t, thiophene-4H), 7.18 (2H, d, 3′-H, 5′-H), 5.11 (2H, s, CH2); m/z 410 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391874B1
Source datasetuspto-grants-2002_05
ORD IDord-c885a4002e8a4a5ba9affeb3203439d5
Source noteuspto-grants-2002_05