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Ethanol → [1,2,4]Triazolo[1,5-a]pyrazin-2-amine

HRID 1022104
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HRID 1022104 반응식
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[NH:7][C:8]([NH:10]C(=O)OCC)=S.Cl.NO.CC[N:21](C(C)C)C(C)C.C(O)C>CO>[N:7]1[C:8]([NH2:10])=[N:21][N:1]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]=12
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참가 물질

6

반응물 4

HCID 702EthanolHCID 81531DiisopropylethylamineHCID 443297Hydroxyamine hydrochlorideHCID 15619487Ethyl N-[(Pyrazin-2-yl)carbamothioyl]carbamate

생성물 1

HCID 13033266[1,2,4]Triazolo[1,5-a]pyrazin-2-amine수율 92%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
65 °C

실험 절차

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 270a (6.00 g, 26.43 mmol, 1.0 eq.), hydroxylamine hydrochloride (3.32 g, 47.52 mmol, 1.8 eq.), DIPEA (12 mL), ethanol (40 mL), and methanol (40 mL). The reaction mixture was stirred at 65° C. for 16 hours. After the reaction was complete, it was cooled to room temperature and concentrated to a volume of around 20 mL under reduced pressure. The resulting suspension was collected by filtration and the solid was washed with 60:1 dichloromethane/ethanol (50 mL) to afford 270b (3.3 g, 92%) as a white solid. MS-ESI: [M+H]+ 136.3. 1H NMR (500 MHz, DMSO-d6) δ 8.84 (d, J=1.0 Hz, 1H), 8.70 (dd, J=1.0, 4.0 Hz, 1H), 7.98 (d, J=5.0 Hz, 1H), 6.47 (s, 2H).

후처리

  1. customA 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser
  2. temperatureit was cooled to room temperature
  3. concentrationconcentrated to a volume of around 20 mL under reduced pressure
  4. filtrationThe resulting suspension was collected by filtration
  5. washthe solid was washed with 60:1 dichloromethane/ethanol (50 mL)

출처 및 근거

ORD 기록
ord-3a86f701399546ccb50441172eeca419
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716274B2

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