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Dimethylformamide → Diisopropylethylamine

HRID 1426495
ノート
印刷プレビュー

反応式

HRID 1426495 の反応式
[N:1]12[CH2:8][CH2:7]C([CH2:5][CH2:6]1)[CH2:3][CH:2]2[C:9](O)=O.S(Cl)(Cl)=O.[CH3:16]N(C)C=O>>[CH2:8]([N:1]([CH:2]([CH3:3])[CH3:9])[CH:6]([CH3:5])[CH3:16])[CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 122169671-Azabicyclo(2.2.2)octane-2-carboxylic acid

生成物 1

HCID 81531Diisopropylethylamine

実験手順

A mixture of 1-azabicyclo[2.2.2]octane-2-carboxylic acid (488 mg), thionyl chloride (5 mL) and N,N-dimethylformamide (23 mg) was stirred at room temperature for 15 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in tetrahydrofuran (5 mL). A mixture of methyl 3-amino-5-[1-(4-methoxybenzyl)-3-methyl-1H-pyrazol-4-yl]thiophene-2-carboxylate and methyl 3-amino-5-[1-(4-methoxybenzyl)-5-methyl-1H-pyrazol-4-yl]thiophene-2-carboxylate (750 mg) produced above, and N-ethyl-N-(1-methylethyl)propan-2-amine (0.916 mL) were added, and the mixture was stirred at 60° C. for 2 hr. Ethyl acetate (20 mL) and water (10 mL) were added to the reaction mixture, and the separated aqueous layer was extracted with ethyl acetate (10 mL×2). The combined organic layers were washed with brine (20 mL) and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by basic silica gel column chromatography (ethyl acetate/hexane) to give the title compound (534 mg) as a colorless oil.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in tetrahydrofuran (5 mL)
  3. additionA mixture of methyl 3-amino-5-[1-(4-methoxybenzyl)-3-methyl-1H-pyrazol-4-yl]thiophene-2-carboxylate and methyl 3-amino-5-[1-(4-methoxybenzyl)-5-methyl-1H-pyrazol-4-yl]thiophene-2-carboxylate (750 mg)

出典と根拠

ORDレコード
ord-b32b06e7dc3e40b482778898f5e8b3cf
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08933069B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート