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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Phenethylamine → 2-(alpha-Methylbenzylamino) pyrazine

HRID 467
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HRID 467 반응식
CC(N)c1ccccc1.Clc1cnccn1>CC(=O)O.CC(=O)O.CC(C)(C)[O-].Cc1ccccc1.[Na+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>CC(Nc1cnccn1)c1ccccc1
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참가 물질

7

반응물 2

HCID 74081-PhenethylamineHCID 73277Chloropyrazine

생성물 1

HCID 219193402-(alpha-Methylbenzylamino) pyrazine수율 42.54%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 634876Binap, (A+-)-촉매HCID 4144353Palladium (II) acetate
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촉매
HCID 1140Toluene용매

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온도
70 °C

실험 절차

To a solution of 1-phenylethanamine (212 mg, 1.75 mmol) and 2-chloropyrazine (200 mg, 1.75 mmol) in toluene (10 mL) while bubbling N2 was added binap (141 mg, 0.23 mmol), sodium tert-butoxide (235 mg, 2.44 mmol) and palladium(II) acetate (51.0 mg, 0.23 mmol). The reaction mixure was heated at 70 oC for 3 hours. The reaction was concentrated, partitioned between ethyl acetate and water. The aqueous phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated. The crude material was loaded on a 40g silica gel column and purified on a Teledyne Isco instrument, eluting with 20% to 70% ethyl acetate in heptane to provide N-(1-phenylethyl)pyrazin-2-amine (148 mg, 42.5 %) as a solid.

출처 및 근거

ORD 기록
ord-74ae5f362208460ebf2f7ad1b936b06b
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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