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5-Bromo-2-methoxybenzonitrile → (R)-5-(2-(tert-butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrile

HRID 306
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HRID 306 반응식
COc1ccc(Br)cc1C#N.C[C@H](CN)O[Si](C)(C)C(C)(C)C>CC(=O)O.CC(=O)O.CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.Cc1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>COc1ccc(NC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1C#N
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참가 물질

7

반응물 2

HCID 44185605-Bromo-2-methoxybenzonitrileHCID 59302513(R)-2-(tert-butyldimethylsilyloxy)propan-1-amine

생성물 1

HCID 58464488(R)-5-(2-(tert-butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrile수율 47.64%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 4144353Palladium (II) acetate촉매
HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
촉매
HCID 1140Toluene용매

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온도
120 °C

실험 절차

PdOAc2 (0.529 g, 2.36 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (1.124 g, 2.36 mmol) were added in one portion to a degassed solution of 5-bromo-2-methoxybenzonitrile (5 g, 23.58 mmol), (R)-2-(tert- butyldimethylsilyloxy)propan-1-amine (5.36 g, 28.30 mmol) and cesium carbonate (11.52 g, 35.37 mmol) in toluene (100 mL) at 20°C under nitrogen. The resulting suspension was stirred at 120 °C for 50 hours. The reaction mixture was diluted with EtOAc (150 mL) and water (150 mL) and the biphasic mixture was filtered through celite. The organic layer was separated and washed sequentially with water (150 mL) and saturated brine (150 mL). The organic layer was evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford (R)-5-(2-(tert- butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrile (3.60 g, 47.6 %) as a pale yellow oil.

출처 및 근거

ORD 기록
ord-3a15989581314d86a106f9d713384402
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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