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Potassium Carbonate → 1-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-one

HRID 1051901
ノート
印刷プレビュー

反応式

HRID 1051901 の反応式
ClC1C=CC(B(O)O)=CC=1.C(=O)([O-])[O-].[K+].[K+].BrC1N=C(CN2CCCC2=O)SC=1.[Cl:30][C:31]1[CH:36]=[CH:35][C:34]([C:37]2[N:38]=[C:39]([CH2:52][N:53]3[CH2:57][CH2:56][CH2:55][C:54]3=[O:58])[S:40][C:41]=2C2C=CC(S(N)(=O)=O)=CC=2)=[CH:33][CH:32]=1>C1(C)C=CC=CC=1.C(O)C>[Cl:30][C:31]1[CH:36]=[CH:35][C:34]([C:37]2[N:38]=[C:39]([CH2:52][N:53]3[CH2:57][CH2:56][CH2:55][C:54]3=[O:58])[S:40][CH:41]=2)=[CH:33][CH:32]=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 11430Potassium CarbonateHCID 742994-Chlorophenylboronic acidHCID 717353994-(4-(4-Chlorophenyl)-2-((2-oxopyrrolidin-1-yl)methyl)thiazol-5-yl)benzenesulfonamideHCID 89813516HCID 89813516、化合物

生成物 1

HCID 898133351-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-one収率 86.6%

試薬・触媒・溶媒 2

HCID 702
Ethanol
溶媒
HCID 1140Toluene溶媒

反応条件

温度
97.5 °C

実験手順

(4-chlorophenyl) boronic acid (0.22 g, 1.42 mmol) and potassium carbonate (0.41 g, 2.97 mmol) were added to a solution of 1-((4-bromothiazol-2-yl)methyl)pyrrolidin-2-one (Step-1 of Compound 103, 0.31 g, 1.18 mmol) in a mixture of toluene:ethanol (5:15 ml) in a tube at 25° C. Nitrogen gas was bubbled through the reaction mixture for 15 minutes. Tetrakis(triphenylphosphine)(0)palladium (0.07 g, 0.06 mmol) was then added to the reaction mixture under nitrogen atmosphere and the tube was sealed. The reaction mixture was heated at 95-100° C. for lhr under stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and filtered through celite. The celite cake was washed with ethanol (20 ml). The combined filtrate was concentrated under reduced pressure to obtain a crude product, which was then purified by column chromatography using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.3 g, 86.6%).

後処理

  1. customat 25° C
  2. customNitrogen gas was bubbled through the reaction mixture for 15 minutes
  3. customthe tube was sealed
  4. temperatureThe reaction mixture was then cooled to 25° C.
  5. filtrationfiltered through celite
  6. washThe celite cake was washed with ethanol (20 ml)
  7. concentrationThe combined filtrate was concentrated under reduced pressure
  8. customto obtain a crude product, which
  9. customwas then purified by column chromatography

出典と根拠

ORDレコード
ord-a97c1b8094254b22a7901fc5afea14ec
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09388196B2

反応ノート

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