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Potassium Carbonate → 2-(4-fluorophenyl)-N-methyl-6-(methylsulfonamido)-5-(prop-1-en-2-yl)furo[2,3-b]pyridine-3-carboxamide

HRID 2190176
ノート
印刷プレビュー

反応式

HRID 2190176 の反応式
[CH2:1]=[C:2]([Mg]Br)[CH3:3].B(OC(C)C)(OC(C)C)OC(C)C.C([O-])([O-])=O.[K+].[K+].[F:25][C:26]1[CH:31]=[CH:30][C:29]([C:32]2[O:46][C:35]3=[N:36][C:37]([NH:41][S:42]([CH3:45])(=[O:44])=[O:43])=[C:38](I)[CH:39]=[C:34]3[C:33]=2[C:47]([NH:49][CH3:50])=[O:48])=[CH:28][CH:27]=1>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>[F:25][C:26]1[CH:31]=[CH:30][C:29]([C:32]2[O:46][C:35]3=[N:36][C:37]([NH:41][S:42]([CH3:45])(=[O:44])=[O:43])=[C:38]([C:2]([CH3:3])=[CH2:1])[CH:39]=[C:34]3[C:33]=2[C:47]([NH:49][CH3:50])=[O:48])=[CH:28][CH:27]=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 4

HCID 11430Potassium CarbonateHCID 21531Triisopropyl borateHCID 580523242-(4-fluorophenyl)-5-iodo-N-methyl-6-(methylsulfonamido)furo[2,3-b]pyridine-3-carboxamideHCID 178456138HCID 178456138、化合物

生成物 1

HCID 580523332-(4-fluorophenyl)-N-methyl-6-(methylsulfonamido)-5-(prop-1-en-2-yl)furo[2,3-b]pyridine-3-carboxamide収率 73%

試薬・触媒・溶媒

1
HCID 178418397HCID 178418397、化合物触媒

反応条件

温度
0 °C

実験手順

To prop-1-en-2-ylmagnesium bromide (0.5 M THF solution, 6.1 ml, 5 eq.) in a heatgun-dried microwave tube at 0° C. was added triisopropyl borate (0.71 ml, 5 eq.). The mixture was stirred at 0° C. for 15 min and warmed to rt. K2CO3 (2 M aq. solution, 1.5 ml, 5 eq.) was added. The mixture was stirred at rt for 15 min. 2-(4-Fluorophenyl)-5-iodo-N-methyl-6-(methylsulfonamido)furo[2,3-b]pyridine-3-carboxamide (300 mg, 1 eq.) and Pd(PPh3)4 (106 mg, 0.15 eq.) were added. The mixture was degassed, stirred in a microwave reactor at 120° C. for 20 min and cooled. Water was added followed by LiOH (1 M aq. solution, 1.8 ml). The mixture was washed with ether. (It took a long time for layers to settle. There may be a solid meta-phase which can be filtered out as pure product.) Aq. layer was acidified to pH 3.5 using saturated citric acid. Precipitate was filtered, washed with water and lyophilized to give the title compound as an off-white solid (180 mg, 73%). MS (ESI) m/z 404.2 (M+1). Retention time=1.23 min (Method A).

後処理

  1. temperaturewarmed to rt
  2. stirringThe mixture was stirred at rt for 15 min
  3. customThe mixture was degassed
  4. stirringstirred in a microwave reactor at 120° C. for 20 min
  5. temperaturecooled
  6. additionWater was added
  7. washThe mixture was washed with ether
  8. filtrationcan be filtered out as pure product
  9. filtrationPrecipitate was filtered
  10. washwashed with water

出典と根拠

ORDレコード
ord-7d1c40db8f27497eb80369e553ca1814
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324239B2

反応ノート

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