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isoquinolin-N-oxide → HCID 178518882, 화합물

HRID 1987641
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HRID 1987641 반응식
[CH:1]1([C:4]2[CH2:8][C:7](=[O:9])[NH:6][N:5]=2)[CH2:3][CH2:2]1.[CH:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][N+:11]=1[O-]>C(OC(=O)C)(=O)C>[CH:1]1([C:4]2=[N:5][NH:6][C:7](=[O:9])/[C:8]/2=[C:10]2\[NH:11][CH:12]=[CH:13][C:14]3[C:19]\2=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 290378isoquinolin-N-oxideHCID 220594943-cyclopropyl-4,5-dihydro-1H-pyrazol-5-one

생성물 1

HCID 178518882HCID 178518882, 화합물

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

3-Cyclopropyl-1H-pyrazol-5(4H)-one (0.03 g, 0.27 mmol) and isoquinoline N-oxide (0.04 g, 0.27 mmol) were stirred in acetic anhydride (0.5 mL) for 30-40 minutes. The reaction mixture was concentrated and purified by LC-MS to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.78-0.86 (m, 4H) 1.77-1.86 (m, 1H) 7.91 (t, J=7.71 Hz, 1H) 8.10 (t, J=7.58 Hz, 1H) 8.26 (d, J=8.59 Hz, 3H) 8.58 (d, J=6.57 Hz, 1H); ESI-MS: m/z calc'd for C15H13N3O 251.28. found 252.2 (M+H)+.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. custompurified by LC-MS

출처 및 근거

ORD 기록
ord-061c05521a374d2fa0e516b7609e6cf7
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07550598B2

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