HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306710Generated: November 3, 2026
2-(Tributylstannyl)pyridine → HCID 22609779, compound
https://huagongshe.com/reaction/2306710
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | (6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amine | HCID 1569266 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22609779 | HCID 22609779 | 56% |
Reaction Steps
The (4-benzyloxy-phenyl)-(6-bromoquinazolin-4-yl)-amine (200 mg, 0.49 mmol), 2-(tributylstannyl)pyridine (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 9 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 (110 mg, 56%) as a pale yellow solid; δH [2H6]-DMSO 9.99 (1H, b, NH), 9.18 (1H, s, 5-H), 8.76 (1H, d, pyridine-H), 8.60 (1H, d, 7-H), 8.54 (1H, s, 2-H), 8.23 (1H, d, pyridine-H), 8.00 (1H, t, pyridine-H), 7.87 (1H, d, 8-H), 7.70 (2H, d, 2′-H, 6′-H), 7.53-7.31 (6H, m, 5×Ph-H, pyridine-H), 7.09 (2H, d, 3′-H, 5′-H), 5.14 (2H, s, CH2); m/z 405 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06828320B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-cb8717d2f60e4447ac3c727ae6c4e581 |
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| Source note | uspto-grants-2004_12 |
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