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tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate

HRID 433
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HRID 433 반응식
CC(C)(C)OC(=O)N1CCNCC1.Cc1ncccc1Br>CC(=O)O.CC(=O)O.CC(C)(C)[O-].CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.Cc1ccccc1.[Na+].[Pd]>Cc1ncccc1N1CCN(C(=O)OC(C)(C)C)CC1
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참가 물질

7

반응물 2

HCID 143452tert-Butyl piperazine-1-carboxylateHCID 12010033-Bromo-2-methylpyridine

생성물 1

HCID 68106327Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate수율 82.86%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 4144353Palladium (II) acetate촉매
HCID 16217985
2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl
촉매
HCID 1140Toluene용매

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온도
100 °C

실험 절차

RuPhos (0.543 g, 1.16 mmol) and palladium (II) acetate (0.131 g, 0.58 mmol) were suspended in toluene (15 mL) at ambient temperature. The resulting mixture was degassed and purged several times and warmed to 50°C under nitrogen for 20 mins. In a separate vessel were mixed 3-bromo-2-methylpyridine (2 g, 11.63 mmol), tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate (2.67 g, 83 %), sodium tertbutoxide (1.676 g, 17.44 mmol) and toluene. The mixture was degassed and purged with nitrogen several times and warmed to 50°C. The catalyst solution was added to the reaction vessel and the resulting mixture degassed and purged wtih nitrogen. The reaction was heated at 100°C overnight. The reaction mixture was allowed to cool to ambient temperature and filtered through GF/F paper, washing with MeOH. The filtrate was concentrated to provide the crude material. This was purified by flash silica chromatography, elution gradient 20 to 70% EtOAc in heptane. Pure fractions were evaporated to dryness to afford tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate (2.67 g, 83 %) as a pale yellow oil.

출처 및 근거

ORD 기록
ord-4147e405915e4ea7b4607546c536b535
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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