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Cesium carbonate → HCID 44224458、化合物

HRID 2068621
ノート
印刷プレビュー

反応式

HRID 2068621 の反応式
Br[C:2]1[S:6][CH:5]=[C:4]([C:7]([N:9]2[CH2:15][CH2:14][CH2:13][C:12]([CH3:17])([CH3:16])[CH2:11][CH2:10]2)=[O:8])[CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C(OC(=O)C[N:29]1[CH:33]=[C:32](B2OC(C)(C)C(C)(C)O2)[CH:31]=[N:30]1)C>COCCOC.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd]>[CH3:16][C:12]1([CH3:17])[CH2:13][CH2:14][CH2:15][N:9]([C:7]([C:4]2[CH:3]=[C:2]([C:32]3[CH:33]=[N:29][NH:30][CH:31]=3)[S:6][CH:5]=2)=[O:8])[CH2:10][CH2:11]1
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 3

HCID 10796Cesium carbonateHCID 162183851-(Ethoxycarbonylmethyl)-1H-pyrazole-4-boronic acid pinacol esterHCID 44227299HCID 44227299、化合物

生成物 1

HCID 44224458HCID 44224458、化合物収率 5%

試薬・触媒・溶媒 2

HCID 11979704Tetrakis(triphenylphosphine)palladium触媒
HCID 8071
1,2-Dimethoxyethane
溶媒

反応条件

温度
140 °C

実験手順

(5-Bromo-thiophen-3-yl)-(4,4-dimethyl-azepan-1-yl)-methanone (0.31 g, 0.99 mmol), together with caesium carbonate (0.483 g, 1.49 mmol),), [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-acetic acid ethyl ester (0.28 g, 1.0 mmol) and palladium tetrakis(triphenylphosphine) (114 mg, 0.1 mmol) were taken up in DME (9 mL), IMS (2 mL) and water (1 mL) and the vessel was purged with argon. The reaction mixture was heated by microwave irradiation to 140° C. for 20 minutes and then diluted with water then treated with dilute HCl (pH adjusted to 4) and extracted with DCM (×3). The organic solution was dried over sodium sulfate, filtered and the solvent evaporated. The residue was purified by chromatography on a silica II cartridge, eluting with 50 then 100% ethyl acetate in cyclohexane then 5% acetic acid in ethyl acetate. The residue was further purified by HPLC, eluting with 10%-98% acetonitrile in water (0.1% formic acid) and the fractions containing desired product were freeze-dried to give the title compound (0.015 g). LCMS m/z 362.24 [M+H]+ R.T.=8.84 min (Analytical Method 2).

後処理

  1. customIMS (2 mL) and water (1 mL) and the vessel was purged with argon
  2. additiondiluted with water
  3. additionthen treated with dilute HCl (
  4. extractionextracted with DCM (×3)
  5. dry with materialThe organic solution was dried over sodium sulfate
  6. filtrationfiltered
  7. customthe solvent evaporated
  8. customThe residue was purified by chromatography on a silica II cartridge
  9. washeluting with 50
  10. customThe residue was further purified by HPLC
  11. washeluting with 10%-98% acetonitrile in water (0.1% formic acid)
  12. additionthe fractions containing desired product
  13. customwere freeze-dried

出典と根拠

ORDレコード
ord-655f885c123c48e1b44eb7f0f8a6343f
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08299063B2

反応ノート

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