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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306714Generated: November 2, 2026

1,4-Dioxane → Isohexane ethyl acetate

https://huagongshe.com/reaction/2306714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant(6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amineHCID 1569266—
Reactant1-methyl-5-(tributylstannyl)-1H-1,2,3-triazoleHCID 22609826—
CatalystHCID 178418476HCID 178418476—
ProductIsohexane ethyl acetateHCID 21882781—

Reaction Steps

The (4-benzyloxy-phenyl)-(6-bromoquinazolin-4-yl)-amine (250 mg, 0.62 mmol), 1-methyl-5-(tributylstannyl)-1,2,3-triazole (300 mg, 0.81 mmol) and bis(triphenylphosphine)palladium(II) chloride (catalytic) were dissolved in dioxan (10 ml) and heated at reflux under nitrogen for 48 hr. The solvent was removed from the cooled reaction under vacuum, and the residue was triturated with iso-hexane. The resulting material was dissolved in ethyl acetate, filtered and the filtrate evaporated to dryness. Trituration with ethyl acetate/iso-hexane gave the product (115 mg, 45%) as a beige solid; δH [2H6]-DMSO 9.90 (1H, b, NH), 8.76 (1H, s, 5-H), 8.61 (1H, s, 2-H), 8.10 (2H, m, 7-H, triazole-H), 7.92 (1H, d, 8-H), 7.70 (2H, d, 2′-H, 6′-H), 7.58-7.38 (5H, m, 5×Ph-H), 7.12 (2H, d, 3′-H, 5′-H), 5.19 (2H, s, CH2), 4.22 (3H, s, CH3); m/z 409 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828320B2
Source datasetuspto-grants-2004_12
ORD IDord-9d32a2ab53ac4cb9ade4cbe54ea047f9
Source noteuspto-grants-2004_12