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Thiazolidinedione → HCID 58312813、化合物

HRID 1751181
ノート
印刷プレビュー

反応式

HRID 1751181 の反応式
Cl[C:2]1[N:7]=[C:6]([CH:8]=O)[CH:5]=[C:4]([O:10][CH2:11][CH2:12][O:13][CH3:14])[N:3]=1.[S:15]1[CH2:19][C:18](=[O:20])[NH:17][C:16]1=[O:21].[C:22]1([CH3:34])[CH:27]=[CH:26][C:25]([N:28]2[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]2)=[CH:24][CH:23]=1>C(O)C>[CH3:14][O:13][CH2:12][CH2:11][O:10][C:4]1[N:3]=[C:2]([N:31]2[CH2:32][CH2:33][N:28]([C:25]3[CH:26]=[CH:27][C:22]([CH3:34])=[CH:23][CH:24]=3)[CH2:29][CH2:30]2)[N:7]=[C:6](/[CH:8]=[C:19]2/[C:18](=[O:20])[NH:17][C:16](=[O:21])[S:15]/2)[CH:5]=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

5

反応物 3

HCID 5437ThiazolidinedioneHCID 831131-(p-Tolyl)piperazineHCID 58312971HCID 58312971、化合物

生成物 1

HCID 58312813HCID 58312813、化合物収率 104.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

Crude 2-chloro-6-(2-methoxyethoxy)pyrimidine-4-carbaldehyde (sad105-052, 41.9 mg) was dissolved in ethanol (1.5 mL) and was added to a 10 mL vial containing the thiazolidine-dione (21.3 mg, 0.18 mmol) and the 1-(p-tolyl)piperazine (39.3 mg, 0.18 mmol). The reaction mixture was shaken at 80° C. for 15.5 h. LC-MS showed a peak with the desired mass at 2.18 min (M+1=456). The solvent was concentrated under reduced pressure and the residue was dissolved in EtOAc (20 mL) and washed with saturated NaHCO3 (10 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to provide 85.7 mg of brown oil. Purification by flash chromatography (SiO2,10 g, Hexanes/EtOAc 9:1 to 6:4 to 1:1) provided 11.5 mg (13.9% 2 steps, 83 mg theoretical) of pure (Z)-5-((6-(2-methoxyethoxy)-2-(4-(p-tolyl)piperazin-1-yl)pyrimidin-4-yl)methylene)thiazolidine-2,4-dione as a yellow solid.

後処理

  1. additionwas added to a 10 mL
  2. customat 2.18 min
  3. concentrationThe solvent was concentrated under reduced pressure
  4. dissolutionthe residue was dissolved in EtOAc (20 mL)
  5. washwashed with saturated NaHCO3 (10 mL)
  6. dry with materialThe organic layer was dried over Na2SO4
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-4cfbfcd1162a4d5faa23986ae9af53cd
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09157077B2

反応ノート

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