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Diglycolamine → HCID 178518154、化合物

HRID 1620479
ノート
印刷プレビュー

反応式

HRID 1620479 の反応式
[NH2:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][OH:7].S=[C:9]1[CH2:13][S:12][C:11](=[O:14])[NH:10]1.[F:15][C:16]([F:37])([F:36])[C:17]1[CH:31]=[C:30]([C:32]([F:35])([F:34])[F:33])[CH:29]=[CH:28][C:18]=1[CH2:19][N:20]1[CH2:25][CH2:24][CH:23]([CH:26]=O)[CH2:22][CH2:21]1.CC(C)([O-])C.[K+].[Cl-].[NH4+]>C(O)C.C(OCC)(=O)C>[F:37][C:16]([F:15])([F:36])[C:17]1[CH:31]=[C:30]([C:32]([F:35])([F:34])[F:33])[CH:29]=[CH:28][C:18]=1[CH2:19][N:20]1[CH2:25][CH2:24][CH:23](/[CH:26]=[C:13]2/[C:9]([NH:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][OH:7])=[N:10][C:11](=[O:14])[S:12]/2)[CH2:22][CH2:21]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 13578DiglycolamineHCID 25517Ammonium ChlorideHCID 15395954-Sulfanylidene-1,3-thiazolidin-2-oneHCID 23665647Potassium tert-butoxideHCID 866786631-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde

生成物 1

HCID 178518154HCID 178518154、化合物

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 2-(2-aminoethoxy)ethanol (4.24 mL) in ethanol (30 mL) was added 4-thioxo-1,3-thiazolidin-2-one (5.65 g), and the mixture was stirred at room temperature for 4 hr. To the reaction mixture were added 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (12 g) and potassium tert-butoxide (4.76 g), and the mixture was stirred at 80° C. for 3 hr. The reaction mixture was cooled to room temperature, saturated aqueous ammonium chloride solution/ethyl acetate were added, and the organic layer was separated, washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) to give the title compound (4.3 g).

後処理

  1. stirringthe mixture was stirred at 80° C. for 3 hr
  2. temperatureThe reaction mixture was cooled to room temperature
  3. customthe organic layer was separated
  4. washwashed with water and saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (methanol/ethyl acetate)

出典と根拠

ORDレコード
ord-4e1b1eeb1ab54c96af950616e8c0fa15
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08772277B2

反応ノート

読み込み中…

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