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Cesium carbonate → Ethyl 5-(4-fluorobenzamido)-2-[methyl(quinolin-6-yl)amino]thiazole-4-carboxylate

HRID 512544
ノート
印刷プレビュー

反応式

HRID 512544 の反応式
Br[C:2]1[S:3][C:4]([NH:12][C:13](=[O:21])[C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)=[C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[N:6]=1.CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:70][NH:71][C:72]1[CH:73]=[C:74]2[C:79](=[CH:80][CH:81]=1)[N:78]=[CH:77][CH:76]=[CH:75]2>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[F:20][C:17]1[CH:18]=[CH:19][C:14]([C:13]([NH:12][C:4]2[S:3][C:2]([N:71]([CH3:70])[C:72]3[CH:73]=[C:74]4[C:79](=[CH:80][CH:81]=3)[N:78]=[CH:77][CH:76]=[CH:75]4)=[N:6][C:5]=2[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:21])=[CH:15][CH:16]=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

7

反応物 4

HCID 10796Cesium carbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 12765505N-methylquinolin-6-amineHCID 86703378Ethyl 2-bromo-5-(4-fluorobenzamido)-thiazole-4-carboxylate

生成物 1

HCID 86703379Ethyl 5-(4-fluorobenzamido)-2-[methyl(quinolin-6-yl)amino]thiazole-4-carboxylate

試薬・触媒・溶媒 2

HCID 9811564Bis(dibenzylideneacetone)palladium触媒HCID 1140Toluene溶媒

反応条件

温度
110 °C

実験手順

To a solution of ethyl 2-bromo-5-(4-fluorobenzamido)-thiazole-4-carboxylate (0.2 g, 0.50 mmol) in toluene (10 mL) was added Xantphos (0.061 g, 0.10 mmol) and Pd2(dba)3 (0.048 g, 0.040 mmol) under argon gas. To this suspension, cesium carbonate (0.344 g, 0.90 mmol) and N-methylquinolin-6-amine (0.084 g, 0.53 mmol) were added, and the mixture was heated at 110° C. for 16 h. The reaction mixture was filtered through a bed of Celite, and the celite pad was washed with ethyl acetate (3×5 mL). The filtrate was concentrated, and the crude residue was purified by silica gel column chromatography eluted with 50% EtOAc in hexane to give 0.14 g (58% yiled) of the titled compound.

後処理

  1. filtrationThe reaction mixture was filtered through a bed of Celite
  2. washthe celite pad was washed with ethyl acetate (3×5 mL)
  3. concentrationThe filtrate was concentrated
  4. customthe crude residue was purified by silica gel column chromatography
  5. washeluted with 50% EtOAc in hexane

出典と根拠

ORDレコード
ord-60225ea68c3c418a8d6f03ad8992ada3
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09102637B2

反応ノート

読み込み中…

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