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Bromine → 2-Bromo-5,6-dihydrothieno(2,3-c)pyridin-7(4H)-one

HRID 2091574
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HRID 2091574 반응식
[S:1]1[C:5]2[C:6](=[O:10])[NH:7][CH2:8][CH2:9][C:4]=2[CH:3]=[CH:2]1.[Br:11]Br>CC(O)=O.O>[Br:11][C:2]1[S:1][C:5]2[C:6](=[O:10])[NH:7][CH2:8][CH2:9][C:4]=2[CH:3]=1
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참가 물질

5

반응물 2

HCID 24408BromineHCID 218153465,6-Dihydrothieno[2,3-c]pyridin-7(4H)-one

생성물 1

HCID 513419322-Bromo-5,6-dihydrothieno(2,3-c)pyridin-7(4H)-one수율 73%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

실험 절차

To a 0° C. solution of 5,6-dihydrothieno[2,3-c]pyridin-7(4H)-one (820 mg, 5.36 mmol) in HOAc (7 mL) and (5 mL) water was added bromine (303 μL, 5.9 mmol) and the reaction was stirred 1.5 h. The reaction was diluted in water (30 mL) and the aqueous mixture was extracted with EtOAc (2×50 mL). The combined organics were washed with 5% aq. Na2SO3 (40 mL), sat. aq. NaHCO3 (40 mL), and brine (40 mL). The organic was dried over Na2SO4, then filtered and concentrated. After purification by flash chromatography over silica gel (50-100% EtOAc/hexane eluent), 2-bromo-5,6-dihydrothieno[2,3-c]pyridin-7(4H)-one (906 mg, 73% yield) was isolated as a white solid. 1H NMR (400 MHz, METHANOL-d4) δ ppm 7.10 (s, 1H), 3.55 (t, J=7.0 Hz, 2H), 2.88 (t, J=7.0 Hz, 2H); MS (EI) m/z=233.1 [M+1]+.

후처리

  1. extractionthe aqueous mixture was extracted with EtOAc (2×50 mL)
  2. washThe combined organics were washed with 5% aq. Na2SO3 (40 mL), sat. aq. NaHCO3 (40 mL), and brine (40 mL)
  3. dry with materialThe organic was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customAfter purification by flash chromatography over silica gel (50-100% EtOAc/hexane eluent)

출처 및 근거

ORD 기록
ord-f98ad80ca9074e5aa58ee444d3859237
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08440652B2

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