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2-Chloro-4-aminopyrimidine → 2-chloro-N-pyridin-4-ylpyrimidin-4-amine

HRID 278
ノート
印刷プレビュー

反応式

HRID 278 の反応式
Ic1ccncc1.Nc1ccnc(Cl)n1>C1CCCC1.C1COCCO1.CC(=O)O.CC(=O)O.CC(C1CCCC1P(C1CCCCC1)C1CCCCC1)P(C(C)(C)C)C(C)(C)C.O=C([O-])[O-].[Cs+].[Cs+].[Fe].[Pd]>Clc1nccc(Nc2ccncc2)n1
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 3457522-Chloro-4-aminopyrimidineHCID 6094924-Iodopyridine

生成物 1

HCID 223096862-chloro-N-pyridin-4-ylpyrimidin-4-amine収率 45.34%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 4144353Palladium (II) acetate触媒
HCID 144543273
(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-
触媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
80 °C

実験手順

diacetoxypalladium (0.035 g, 0.15 mmol) was added to a mixture of 2-chloropyrimidin-4-amine (0.250 g, 1.93 mmol), 4-iodopyridine (0.396 g, 1.93 mmol), cesium carbonate (0.755 g, 2.32 mmol) and (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (0.105 g, 0.19 mmol) in 1,4-dioxane (10 mL) and the reaction mixture stirred for 18 hours at 80 °C under nitrogen. EtOAc (50ml) was added to the reaction mixture and then the organics washed with water (3 x 50ml), brine (50ml) and then dried over MgSO4. The organics were then evaporated in vacuo to give the crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Pure fractions were evaporated to dryness to afford 2-chloro-N-(pyridin-4-yl)pyrimidin-4-amine (0.181 g, 45.3 %) as an orange solid.

出典と根拠

ORDレコード
ord-0cc10dc98bd741d3bb43f77d99dd2224
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

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