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Cesium carbonate → N-(3,4-Dimethoxybenzyl)-3',5'-dimethyl-4-pyridin-3-ylbiphenyl-3-carboxamide

HRID 1948558
ノート
印刷プレビュー

反応式

HRID 1948558 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]([C:22]2[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=2)=[C:6]([CH:21]=1)[C:7]([NH:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[C:13]([O:19][CH3:20])[CH:12]=1)=[O:8].[CH3:28][C:29]1[CH:30]=[C:31](B(O)O)[CH:32]=[C:33]([CH3:35])[CH:34]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C.O.CCOC(C)=O.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>[CH3:20][O:19][C:13]1[CH:12]=[C:11]([CH:16]=[CH:15][C:14]=1[O:17][CH3:18])[CH2:10][NH:9][C:7]([C:6]1[CH:21]=[C:2]([C:31]2[CH:32]=[C:33]([CH3:35])[CH:34]=[C:29]([CH3:28])[CH:30]=2)[CH:3]=[CH:4][C:5]=1[C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1)=[O: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

8

反応物 3

HCID 10796Cesium carbonateHCID 27343493,5-Dimethylphenylboronic acidHCID 584084115-Bromo-N-(3,4-dimethoxybenzyl)-2-pyridin-3-ylbenzamide

生成物 1

HCID 58408399N-(3,4-Dimethoxybenzyl)-3',5'-dimethyl-4-pyridin-3-ylbiphenyl-3-carboxamide

試薬・触媒・溶媒 4

HCID 178418807HCID 178418807、化合物触媒
HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
150 °C

実験手順

A solution of 1-3 (90 mg, 0.211 mmol, 1.0 equiv) in DMF (2 ml) in a microwave vial was treated with the 3,5-dimethylphenyl boronic acid (34.7 mg, 0.232 mmol, 1.1 equiv), cesium carbonate (0.632 mL of a 1M solution in water, 0.632 mmol, 3.0 equiv), and PdCl2(dppf)-CH2Cl2 adduct (17.20 mg, 0.021 mmol, 0.1 equiv). The mixture was heated to 150° C. in a microwave reactor for 10 minutes. The mixture was cooled to room temperature and diluted with EtOAc. The organic solution was washed with sat. aq. NH4Cl, dried over Na2SO4, filtered and concentrated. The crude material was purified by gradient elution on silica gel (0 to 100% EtOAc in hexanes) to yield impure material which was precipitated from ether/hexanes and filtered. The solid was isolated to afford the product (1-4) as a tan solid. HRMS [M+H] C26H27N5O3 calc'd 453.2173. found 453.2178.

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. washThe organic solution was washed with sat. aq. NH4Cl
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified by gradient elution on silica gel (0 to 100% EtOAc in hexanes)
  7. customto yield impure material which
  8. customwas precipitated from ether/hexanes
  9. filtrationfiltered
  10. customThe solid was isolated

出典と根拠

ORDレコード
ord-11298d43abc84d63bd1746caf6c524a7
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399494B2

反応ノート

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