HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936783Generated: November 1, 2026
(6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amine → N-[4-(benzyloxy)phenyl]-6-(1-methyl-1H-imidazol-5-yl)quinazolin-4-amine
https://huagongshe.com/reaction/1936783
Participants
| Role | Name | HCID | Charge |
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| Reactant | (6-Bromoquinazolin-4-yl)[4-(phenylmethoxy)phenyl]amine | HCID 1569266 | — |
| Reactant | 1-Methyl-5-(tri-n-butylstannyl)imidazole | HCID 10915651 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-(benzyloxy)phenyl]-6-(1-methyl-1H-imidazol-5-yl)quinazolin-4-amine | HCID 22609863 | 90% |
Reaction Steps
The (4-benzyloxy-phenyl)-(6-bromoquinazolin-4-yl)-amine (1.0 g, 2.46 mmol), 1-methyl-5-(tributylstannyl)imidazole (prepared according to Gaare, K., et al. Acta Chem. Scand. (1993), 47(1), 57-62) (1.25 g, 3.37 mmol) and bis(triphenylphosphine)palladium(II) chloride (catalytic amount) were reacted according to Procedure B in dioxane (50 ml) for 3 hours. The solvent was removed in vacuo, and the solid was washed with i-hexane. The resulting dark solid was suspended in IMS, and undissolved material removed by filtration. The resulting filtrate was concentrated in vacuo to give the product as a pale baige solid (0.90 g, 2.21 mmol, 90%);_δH [2H6]-DMSO 9.69 (1H, b, NH), 8.60 (1H, s, 5-H), 8.55 (1H, s, 2-H), 8.00 (1H, d, 7-H), 7.83 (2H, m, 8-H, imidazole-H), 7.69 (2H, d, 2′-H, 6′-H), 7.52-7.33 (5H, m, 5×Ph-H), 7.22 (1H, s, imidazole-H), 7.09 (2H, d, 3′-H, 5′-H), 5.14 (2H, s, CH2), 3.80 (3H, s, CH3); m/z 408 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391874B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-d95f2f2c457444b197cab9b873b62a32 |
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| Source note | uspto-grants-2002_05 |
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