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Cesium carbonate → cis-N-{4-[(6-bromopyridin-3-yl)oxy]tetrahydrofuran-3-yl}propane-2-sulfonamide

HRID 2360306
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HRID 2360306 반응식
CS(O[C@H:6]1[C@H:10]([O:11][C:12]2[CH:13]=[N:14][C:15]([Br:18])=[CH:16][CH:17]=2)[CH2:9][O:8][CH2:7]1)(=O)=O.[CH3:19][CH:20]([S:22]([NH2:25])(=[O:24])=[O:23])[CH3:21].C(=O)([O-])[O-].[Cs+].[Cs+].C(=O)(O)[O-].[Na+]>C(#N)C>[Br:18][C:15]1[N:14]=[CH:13][C:12]([O:11][C@H:10]2[CH2:9][O:8][CH2:7][C@H:6]2[NH:25][S:22]([CH:20]([CH3:21])[CH3:19])(=[O:24])=[O:23])=[CH:17][CH:16]=1
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참가 물질

6

반응물 4

HCID 10796Cesium carbonateHCID 516892Sodium BicarbonateHCID 3549191Propane-2-sulfonamideHCID 86653036trans-4-[(6-Bromopyridin-3-yl)oxy]tetrahydrofuran-3-yl methanesulfonate

생성물 1

HCID 86653038cis-N-{4-[(6-bromopyridin-3-yl)oxy]tetrahydrofuran-3-yl}propane-2-sulfonamide

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

Trans-4-[(6-bromopyridin-3-yl)oxy]tetrahydrofuran-3-yl methane sulfonate (591.7 mg, 1.75 mmol), propane-2-sulfonamide (647 mg, 5.25 mmol) and cesium carbonate (855 mg, 2.62 mmol) were combined in acetonitrile (8 mL) and subjected to microwave irradiation for 55 minutes at 150° C. The crude reaction mixture was combined with several similar reactions run under the same conditions (total starting material used: 1.527 g, 4.515 mmol) and shaken with saturated aqueous sodium bicarbonate solution (100 mL). The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel chromatography (Gradient: 5% to 40% ethyl acetate in heptane) to provide the title compound. Yield: 382 mg, 1.046 mmol, 23%. 1H NMR (400 MHz, CDCl3) δ 1.34 (d, J=6.8 Hz, 3H), 1.36 (d, J=6.8 Hz, 3H), 3.17 (septet, J=6.8 Hz, 1H), 3.74 (dd, J=9, 9 Hz, 1H), 3.94 (dd, J=10.9, 1.5 Hz, 1H), 4.14 (dd, J=8, 8 Hz, 1H), 4.19 (dd, J=10.9, 4.3 Hz, 1H), 4.27 (m, 1H), 4.84 (m, 1H), 5.66 (d, J=9.9 Hz, 1H), 7.20 (dd, J=8.8, 3.2 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 8.01 (d, J=3.2 Hz, 1H).

후처리

  1. customirradiation for 55 minutes at 150° C
  2. customThe crude reaction mixture
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. dry with materialthe combined organic layers were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified via silica gel chromatography (Gradient: 5% to 40% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-c8ea1e2b359e400f89fd67547a265bb5
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08686043B2

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