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Cesium carbonate → 3-Bromo-4-chloro-5-cyclopropylpyridine

HRID 1521565
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HRID 1521565 반응식
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Br:9])[C:7]=1[Cl:8].[CH:10]1(B(O)O)[CH2:12][CH2:11]1.C(=O)([O-])[O-].[Cs+].[Cs+].O1CCOCC1>O>[Br:9][C:6]1[CH:5]=[N:4][CH:3]=[C:2]([CH:10]2[CH2:12][CH2:11]2)[C:7]=1[Cl:8]
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참가 물질

6

반응물 4

HCID 10796Cesium carbonateHCID 312751,4-DioxaneHCID 8170943,5-Dibromo-4-chloropyridineHCID 2760897Cyclopropylboronic acid

생성물 1

HCID 709778753-Bromo-4-chloro-5-cyclopropylpyridine

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
100 °C

실험 절차

To a stirred solution of 3,5-dibromo-4-chloropyridine (X, 0.5 g, 1.84 mmol) and cyclopropylboronic acid (0.17 g, 2.02 mmol), cesium carbonate (1.19 g, 3.68 mmol) in the mixture of 1,4-dioxan (10 mL) and water (2 mL). The reaction mass was purged with nitrogen for 15 min. Then catalyst Pd (dppf)2Cl2 (0.075 g, 0.09 mmol) was added and allowed to stir at 100° C. for 4 h. The reaction mixture was filtered through Mite bed and filter bed was thoroughly washed with ethyl acetate. The collected organic parts were concentrated under vacuum to afford the crude compound, which was purified by column chromatography using 10-40% ethyl acetate/hexane as an eluent to obtain title compound. MS (M+1): 233.0.

후처리

  1. customThe reaction mass was purged with nitrogen for 15 min
  2. filtrationThe reaction mixture was filtered through Mite bed
  3. filtrationfilter bed
  4. washwas thoroughly washed with ethyl acetate
  5. concentrationThe collected organic parts were concentrated under vacuum
  6. customto afford the crude compound, which
  7. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-cab961102af34701863775feefb14831
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073929B2

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