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1,4-Dioxa-8-azaspiro(4.5)decane → 8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane

HRID 454
ノート
印刷プレビュー

反応式

HRID 454 の反応式
C1CC2(CCN1)OCCO2.COc1cncc(Br)c1>CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.Cc1ccccc1.[Na+].[Pd]>COc1cncc(N2CCC3(CC2)OCCO3)c1
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 674351,4-Dioxa-8-azaspiro(4.5)decaneHCID 8171633-Bromo-5-methoxypyridine

生成物 1

HCID 667422848-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane収率 75.12%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 4144353Palladium (II) acetate触媒
HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
触媒
HCID 1140Toluene溶媒

反応条件

温度
100 °C

実験手順

11/05 2011 07:58:54 +0200 A mixture of 3-bromo-5-methoxypyridine (1.5 g, 7.98 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (1.023 ml, 7.98 mmol), palladium(II) acetate (0.107 g, 0.48 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.228 g, 0.48 mmol) in toluene (38.3 ml) and tBuOH (7.65 ml) was evacuated and flashed with N2 several times. Then sodium 2-methylpropan-2-olate (0.920 g, 9.57 mmol) was added and the reaction mixture was heated to 100°C for 2hrs. LCMS showed complete conversion. Reaction mixture had turned black. The reaction mixture was filtered through celite. The celite was washed with DCM. The combined filtrates were concentrated to yield 2.2g of brown oil, which starts to crystalise patially. Crude NMR showed only little unreacted amine (ca. 14%). The crude was purified by flash: The residue was purified by automated flash chromatography on a 100g column. A gradient from 40% to 100% of EA in Hep over 12CV, 100% EA over 6CV was used as mobile phase. The product was collected using the wavelength 254 nm. 1.5g of desired product were obtained as a light yellow oil.

出典と根拠

ORDレコード
ord-7ce32a5d4abb4826b07e10a8720e8cf8
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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