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Hydrochloric Acid → Ethyl 2-(2-chloropyrimidin-4-yl)-1H-indole-5-carboxylate

HRID 1037576
ノート
印刷プレビュー

反応式

HRID 1037576 の反応式
B([C:4]1[NH:5][C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:8][CH:7]=2)(O)O.C(=O)([O-])[O-].[Na+].[Na+].Cl[C:25]1[N:30]=[CH:29][N:28]=[C:27](Cl)[CH:26]=1.O=O.[ClH:34]>C(O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[Cl:34][C:29]1[N:28]=[C:27]([C:4]2[NH:5][C:6]3[C:11]([CH:12]=2)=[CH:10][C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:8][CH:7]=3)[CH:26]=[CH:25][N:30]=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

9

反応物 5

HCID 313Hydrochloric AcidHCID 977OxygenHCID 10340Sodium CarbonateHCID 709434,6-DichloropyrimidineHCID 59800131HCID 59800131、化合物

生成物 1

HCID 59800134Ethyl 2-(2-chloropyrimidin-4-yl)-1H-indole-5-carboxylate収率 93%

試薬・触媒・溶媒 3

HCID 178418397HCID 178418397、化合物触媒
HCID 702Ethanol溶媒
HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

28 g (114 mmol) of 2-borono-5-ethoxycarbonylindole, 12 g (113 mmol) of sodium carbonate and 17.2 g of 2,4-(113 mmol) dichloropyrimidine were initially charged in 412 ml of ethanol. The clear solution was freed of oxygen by vigorous stirring and passing argon through (20 minutes). At RT, 2.67 g of tetrakis(triphenylphosphine)palladium(0) were added. The mixture was heated to from 65° C. to 70° C. for 2 hours (h). Subsequently, 112 ml of water and 112 ml of 30% hydrochloric acid were added and the mixture was cooled to 0° C. After filtration and drying under reduced pressure, 37.3 g (93% of theory) of ethyl 2-(2-chloropyrimidin-4-yl)-1H-indole-5-carboxylate were obtained (HPLC >96%).

後処理

  1. customthrough (20 minutes)
  2. temperatureThe mixture was heated to from 65° C. to 70° C. for 2 hours (h)
  3. filtrationAfter filtration
  4. customdrying under reduced pressure

出典と根拠

ORDレコード
ord-07799abdaf0643c994312b7c07d58039
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08546567B2

反応ノート

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