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Benzyl Alcohol → 3-(Benzyloxy)-5-bromopyrazin-2-amine

HRID 2174652
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HRID 2174652 반응식
[H-].[Na+].[CH2:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Br[C:12]1[C:13]([NH2:19])=[N:14][CH:15]=[C:16]([Br:18])[N:17]=1>C1COCC1>[CH2:3]([O:10][C:12]1[C:13]([NH2:19])=[N:14][CH:15]=[C:16]([Br:18])[N:17]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 244Benzyl AlcoholHCID 24758Sodium hydrideHCID 6200042-Amino-3,5-dibromopyrazine

생성물 1

HCID 107551623-(Benzyloxy)-5-bromopyrazin-2-amine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

NaH as a 60% dispersion in mineral oil (31.63 mg, 0.7908 mmol) was added to a solution of benzyl alcohol (85.52 mg, 81.84 μL, 0.7908 mmol) in THF (4 mL). After stirring at ambient temperature for 5 minutes, 3,5-dibromopyrazin-2-amine (100 mg, 0.3954 mmol) was added and the mixture was stirred for 1 hour at ambient temperature then heated at 80° C. under microwave conditions for 15 minutes. The reaction mixture was cooled to ambient temperature, concentrated in vacuo and used directly in the next step without further purification.

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후처리

  1. stirringthe mixture was stirred for 1 hour at ambient temperature
  2. temperaturethen heated at 80° C. under microwave conditions for 15 minutes
  3. temperatureThe reaction mixture was cooled to ambient temperature
  4. concentrationconcentrated in vacuo
  5. customused directly in the next step without further purification

출처 및 근거

ORD 기록
ord-8cd361a627474468b542bca9bcb480ec
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062008B2

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