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3-Bromopyridine → tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylate

HRID 511
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HRID 511 반응식
Brc1cccnc1.C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1>C1COCCO1.CC(=O)O.CC(=O)O.CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.O=C([O-])[O-].[Cs+].[Cs+].[Pd]>C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1cccnc1
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참가 물질

7

반응물 2

HCID 122863-BromopyridineHCID 2756811(R)-1-Boc-3-methylpiperazine

생성물 1

HCID 89555981tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylate수율 0%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 4144353Palladium (II) acetate촉매HCID 162179852-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl

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온도
100 °C

실험 절차

diacetoxypalladium (9.34 mg, 0.04 mmol) and RuPhos (0.039 g, 0.08 mmol) were suspended in 1,4 dioxane (5 mL), degassed and stirred at 50 °C for 10 minutes. Then (R)-tert-butyl 3-methylpiperazine-1-carboxylate (0.100 g, 0.50 mmol), 3-bromopyridine (0.040 mL, 0.42 mmol) and cesium carbonate (0.203 g, 0.62 mmol) were added and the reaction mixture was stirred at 100 °C for 16 h. LCMS showed only 5% conversion to desired product. This was part of a screen and Ruphos, sodium tert-butoxide in toluene gave far better conversion so this was abandoned.

출처 및 근거

ORD 기록
ord-a21d6ec12c02473a98dce7de6b637849
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
출처 보기

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촉매
HCID 312751,4-Dioxane용매