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Diglycolamine → HCID 178518154, 화합물

HRID 1620479
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HRID 1620479 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

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

생성물 1

HCID 178518154HCID 178518154, 화합물

시약·촉매·용매

2
HCID 702Ethanol용매HCID 8857Ethyl Acetate용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-4e1b1eeb1ab54c96af950616e8c0fa15
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772277B2

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