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4-Aminocatechol → HCID 178518331, 화합물

HRID 2236920
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HRID 2236920 반응식
CO[CH:3]=[C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7](=[O:14])[NH:6][C:5]1=[O:15].[OH:16][C:17]1[CH:18]=[C:19]([CH:21]=[CH:22][C:23]=1[OH:24])[NH2:20]>CN(C)C=O>[OH:16][C:17]1[CH:18]=[C:19]([NH:20][CH:3]=[C:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:14])[NH:6][C:5]2=[O:15])[CH:21]=[CH:22][C:23]=1[OH:24]
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참가 물질

4

반응물 2

HCID 1517264-AminocatecholHCID 686923374-Methoxymethylene-4H-isoquinoline-1,3-dione

생성물 1

HCID 178518331HCID 178518331, 화합물수율 26.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

반응 조건

온도
115 °C

실험 절차

To a suspension of 4-Methoxymethylene-4H-isoquinoline-1,3-dione (40.6 mg, 0.2 mmol) in N,N-dimethylformamide (0.5 mL) is added 3,4-dihydroxyaniline (25 mg, 0.2 mmol). The reaction mixture is shaken at 115° C. for 1.5 hours. The reaction mixture is diluted to 2 mL with N,N-dimethylformamide and purified by C18 reverse phase HPLC. The pure fractions were combined and concentrated to yield the title compound (15.6 mg).

후처리

  1. custompurified by C18 reverse phase HPLC
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ef615b3ac6004c3f8c4cabdd00a07a56
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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