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4-Quinolinecarboxaldehyde → Ethyl 1,2,3,4-tetrahydro-6-(hydroxy-4-quinolinylmethyl)-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxylate

HRID 131552
ノート
印刷プレビュー

反応式

HRID 131552 の反応式
C([N-]C(C)C)(C)C.[Li+].[CH3:9][N:10]1[C:15](=[O:16])[C:14]2[C:17]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:18][S:19][C:13]=2[N:12]([CH2:25][CH:26]([CH3:28])[CH3:27])[C:11]1=[O:29].[N:30]1[C:39]2[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=2)[C:33]([CH:40]=[O:41])=[CH:32][CH:31]=1>C1COCC1>[OH:41][CH:40]([C:33]1[C:34]2[C:39](=[CH:38][CH:37]=[CH:36][CH:35]=2)[N:30]=[CH:31][CH:32]=1)[C:18]1[S:19][C:13]2[N:12]([CH2:25][CH:26]([CH3:28])[CH3:27])[C:11](=[O:29])[N:10]([CH3:9])[C:15](=[O:16])[C:14]=2[C:17]=1[C:20]([O:22][CH2:23][CH3:24])=[O:21]
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 780724-QuinolinecarboxaldehydeHCID 2724682Lithium diisopropylamideHCID 5282568Ethyl 3-methyl-1-(2-methylpropyl)-2,4-dioxo-1,2,3,4-tetrahydro-thieno[2,3-d]pyrimidine-5-carboxylate

生成物 1

HCID 5282569Ethyl 1,2,3,4-tetrahydro-6-(hydroxy-4-quinolinylmethyl)-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxylate

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

反応条件

温度
-78 °C

実験手順

A solution of lithium diisopropylamide (5.52 g) in anhydrous THF (80 ml) was added dropwise over 1 h to a stirred solution of the product of step c) (8.02 g) and 4-quinolinecarboxaldehyde (8.12 g) in anhydrous THF (80 ml) at −78° C. under nitrogen. The mixture was stirred for a further 1 hour at −78° C. then quenched with glacial acetic acid (10 ml), allowed to warm to room temperature, diluted with saturated sodium bicarbonate solution (100 ml) and extracted into ethyl acetate (2×100 ml). The combined extracts were dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography, eluting with 3:2 ethyl acetate/i-hexane, to give the sub-title compound as a white solid (7.35 g). MS(ESI) 468 {M+H]+. δ 1HCDCl3 0.85 (3H,d), 0.88 (3H,d), 1.43 (3H,t), 2.10-2.16 (1H,m), 3.38 (3H,s), 3.49 (1H,dd), 3.61 (1H, s,br), 3.71 (1H,dd), 4.48 (2H,quartet), 6.78 (1H,s), 7.52 (1H,t), 7.72 (1H,t), 7.83 (1H,d), 7.90 (1H,d), 8.17 (1H,d), 9.02 (1H,d)

後処理

  1. customthen quenched with glacial acetic acid (10 ml)
  2. temperatureto warm to room temperature
  3. additiondiluted with saturated sodium bicarbonate solution (100 ml)
  4. extractionextracted into ethyl acetate (2×100 ml)
  5. dry with materialThe combined extracts were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by column chromatography
  9. washeluting with 3:2 ethyl acetate/i-hexane

出典と根拠

ORDレコード
ord-be19efb468db49dab3ea2944cc2e8b92
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07384950B2

反応ノート

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