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

HRID 1521565
ノート
印刷プレビュー

反応式

HRID 1521565 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-cab961102af34701863775feefb14831
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073929B2

反応ノート

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