Water → 2-Isopropoxy-5-thiazol-2-ylbenzonitrile

HRID 1942636ノート

反応式

HRID 1942636 の反応式
[CH3:1][CH:2]([O:4][C:5]1[CH:12]=[CH:11][C:10](B2OC(C)(C)C(C)(C)O2)=[CH:9][C:6]=1[C:7]#[N:8])[CH3:3].Br[C:23]1[S:24][CH:25]=[CH:26][N:27]=1.C(=O)([O-])[O-].[Cs+].[Cs+].O>C(#N)C.C(OCC)(=O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[CH3:3][CH:2]([O:4][C:5]1[CH:12]=[CH:11][C:10]([C:23]2[S:24][CH:25]=[CH:26][N:27]=2)=[CH:9][C:6]=1[C:7]#[N:8])[CH3:1]

参加物

8

反応条件

温度
120 °C

実験手順

To a suspension of 2-[(1-methylethyl)oxy]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (D39) (109 mg), 2-bromo-1,3-thiazole (93 mg) and cesium carbonate (148 mg) in acetonitrile (3 mL)/water (0.750 mL) stirred under nitrogen was added PdCl2(dppf)-CH2Cl2 adduct (31.0 mg). The reaction vessel was sealed and heated under microwave at 120° C. for 1 h. After cooling the reaction, the reaction mixture was diluted with ethyl acetate, filtered through celite. The filtrate was partitioned between ethyl acetate and water. The organic phase was dried over sodium sulphate and evaporated in vacuo to give the crude product, which was purified by column chromatography to afford 2-[(1-methylethyl)oxy]-5-(1,3-thiazol-2-yl)benzonitrile (D64) (50 mg). MS (ES): C13H12N2OS requires 244. found 245.1 (M+H+).

後処理

  1. customThe reaction vessel was sealed
  2. temperatureAfter cooling
  3. customthe reaction
  4. filtrationfiltered through celite
  5. customThe filtrate was partitioned between ethyl acetate and water
  6. dry with materialThe organic phase was dried over sodium sulphate
  7. customevaporated in vacuo
  8. customto give the crude product, which
  9. customwas purified by column chromatography

出典と根拠

ORDレコード
ord-e977d882c7644fb3b83bd450bb46b14b
出典データセット
uspto-grants-2013_03
特許番号
US08389508B2

反応ノート

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