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Dimethylformamide dimethyl acetal → (E)-6-((dimethylamino)methylene)-2-(methylthio)-7,8-dihydroquinazolin-5(6H)-one

HRID 2383406
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HRID 2383406 반응식
[CH3:1][S:2][C:3]1[N:12]=[CH:11][C:10]2[C:9](=[O:13])[CH2:8][CH2:7][CH2:6][C:5]=2[N:4]=1.[CH3:14][N:15]([CH:17](OC)OC)[CH3:16]>C1(C)C=CC=CC=1>[CH3:14][N:15](/[CH:17]=[C:8]1/[C:9](=[O:13])[C:10]2[CH:11]=[N:12][C:3]([S:2][CH3:1])=[N:4][C:5]=2[CH2:6][CH2:7]/1)[CH3:16]
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참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 137925232-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one

생성물 1

HCID 59490766(E)-6-((dimethylamino)methylene)-2-(methylthio)-7,8-dihydroquinazolin-5(6H)-one수율 60.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 2-(methylthio)-7,8-dihydroquinazolin-5(6H)-one (0.2 g, 1.0 mmol) in toluene (3 mL) was added DMFDMA (0.2 mL, 1.5 mmol). The reaction mixture was then refluxed for 16 hours. The reaction mixture was then cooled to room temperature and concentrated under reduced pressure. The crude compound was purified by flash column chromatography (SiO2, gradient from 100% dichloromethane to 2% methanol in dichloromethane) to give the pure desired product (0.15 g, 60%) as a solid. 1H NMR (CDCl3, 400 MHz): δ 9.0 (s, 1H), 7.72 (s, 1H), 3.18 (s, 6H), 2.98 (t, J=6.0 Hz, 2H), 2.92 (t, J=6.0 Hz, 2H), 2.60 (s, 3H); LCMS [M+H]: 250.

후처리

  1. temperatureThe reaction mixture was then refluxed for 16 hours
  2. concentrationconcentrated under reduced pressure
  3. customThe crude compound was purified by flash column chromatography (SiO2, gradient from 100% dichloromethane to 2% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-0532eaaab2e0428589e5c8528796b9f1
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08263610B2

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