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Phenylhydrazine → HCID 178515216, 화합물

HRID 1907220
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HRID 1907220 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:15]([O:17]CC)=O.[C:20]1([NH:26][NH2:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(N(CC)CC)C>[N+:12]([C:9]1[CH:8]=[CH:7][C:6]2[NH:5][CH:4]=[C:3]3[C:15](=[O:17])[N:26]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)[N:27]=[C:2]3[C:11]=2[CH:10]=1)([O-:14])=[O:13]
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참가 물질

4

반응물 2

HCID 7516PhenylhydrazineHCID 13430300Ethyl 4-chloro-6-nitroquinoline-3-carboxylate

생성물 1

HCID 178515216HCID 178515216, 화합물수율 85%

시약·촉매·용매 1

HCID 8471Triethylamine용매

반응 조건

온도
135 °C

실험 절차

In a vial were added 4a, phenyl hydrazine and triethylamine. The vial was sealed and heated to 135° C. for 12 hours. The product was collected by filtration and was washed with methanol in 85% yield. 1H-NMR (DMSO-d6) δ (ppm): 7.19 (1H, tt, J=7.32, 1.22 Hz), 7.42 (2H, t, J=7.56 Hz), 7.84 (1H, d, J=9.03 Hz), 8.16 (2H, dd, J=8.30, 1.22 Hz), 8.82 (1H, s), 8.89 (1H, d, J=2.44 Hz). m/z 307.3 (MH+).

후처리

  1. customThe vial was sealed
  2. filtrationThe product was collected by filtration
  3. washwas washed with methanol in 85% yield

출처 및 근거

ORD 기록
ord-588e216a14a441a8af153ad8341bc7cb
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598159B2

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