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2-Chloropyridine → N-pyridin-2-yl-1,3-oxazol-2-amine

HRID 576
ノート
印刷プレビュー

反応式

HRID 576 の反応式
Clc1ccccn1.Nc1ncco1>C1COCCO1.CC(=O)O.CC(=O)O.CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>c1ccc(Nc2ncco2)nc1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 79772-ChloropyridineHCID 5585212-Aminooxazole

生成物 1

HCID 67636727N-pyridin-2-yl-1,3-oxazol-2-amine収率 0%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)触媒
HCID 4144353
Palladium (II) acetate
触媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

Palladium(II) acetate (4.49 mg, 0.02 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.017 g, 0.03 mmol) were mixed together in a reaction vessel and evacuated and purged with nitrogen 3 times. Dioxane (1 mL) was added and the resulting mixture was heated to to 50°C for 30 minutes. oxazol-2-amine (0.101 g, 1.20 mmol) together with 2-chloropyridine (0.094 mL, 1.00 mmol) and cesium carbonate (0.456 g, 1.40 mmol) were placed in a second vessel, evacuated and purged with nitrogen 3 times and dioxane (3 mL) was added. The catalyst solution was added and the resulting mixture heated at 100 °C for 16 hours. **No oxazol-2-amine present in proton NMR of crude reaction mixture.** The starting material is decomposing under the reaction conditions, could be the route of the very low productivity in the C-N couplings using these substrates. Only chloropyridine observed in the proton NMR and LCMS of the crude reaction mixture. Conclusion: Experiment abandoned, none of the desired product isolated. .

出典と根拠

ORDレコード
ord-cdacdc2f62e2433897c344ea48603986
出典データセット
750 AstraZeneca ELN dataset
元リンク
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反応ノート

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